{ "version": "https://jsonfeed.org/version/1.1", "title": "Food and drug recalls (FDA)", "home_page_url": "https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts", "description": "Events collected by UnlimitedPipe 0.3.2", "_unlimitedpipe": { "schema": "unlimitedpipe.event/1", "generator": "UnlimitedPipe 0.3.2" }, "items": [ { "id": "bf75fa1992b4ce796a11", "title": "G. L. Mezzetta Inc. Announces Recall of Mezzetta Brand Golden Greek Peperoncini (Medium Heat) Due to Presence of Pest Contaminant in the Jar", "content_text": "For generations, families have trusted Mezzetta products on their tables. We take that trust seriously, which is why we want to share what we know about a voluntary recall involving a specific lot of Mezzetta Greek Peppers and the actions we are taking.", "date_published": "2026-09-23T22:17:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "bf75fa1992b4ce796a11", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/g-l-mezzetta-inc-announces-recall-mezzetta-brand-golden-greek-peperoncini-medium-heat-due-presence", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:30:16Z", "data": { "change": "added", "label": "G. L. Mezzetta Inc. Announces Recall of Mezzetta Brand Golden Greek Peperoncini (Medium Heat) Due to Presence of Pest Contaminant in the Jar", "item_type": "entry", "summary": "added: G. L. Mezzetta Inc. Announces Recall of Mezzetta Brand Golden Greek Peperoncini (Medium Heat) Due to Presence of Pest Contaminant in the Jar", "after": { "title": "G. L. Mezzetta Inc. Announces Recall of Mezzetta Brand Golden Greek Peperoncini (Medium Heat) Due to Presence of Pest Contaminant in the Jar", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/g-l-mezzetta-inc-announces-recall-mezzetta-brand-golden-greek-peperoncini-medium-heat-due-presence", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/g-l-mezzetta-inc-announces-recall-mezzetta-brand-golden-greek-peperoncini-medium-heat-due-presence", "author": "FDA", "published_at": "2026-09-23T22:17:00Z", "updated_at": "2026-09-23T22:17:00Z", "summary": "For generations, families have trusted Mezzetta products on their tables. We take that trust seriously, which is why we want to share what we know about a voluntary recall involving a specific lot of Mezzetta Greek Peppers and the actions we are taking.", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 146, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/g-l-mezzetta-inc-announces-recall-mezzetta-brand-golden-greek-peperoncini-medium-heat-due-presence" }, { "id": "7cd0cff4bf28d65ea726", "title": "Deano’s Pasta Issue Allergy Alert on Undeclared Lobster in Pear and Pecorino Triangoli Ravioli", "content_text": "Deano’s Pasta of Somerville, MA is recalling approximately 20 lbs. of Pear and Pecorino Triangoli Ravioli, because it may contain undeclared Lobster. People who have an allergy or severe sensitivity to Crustacean Shellfish (Lobster) run the risk of serious or life-threatening allergic reaction if th", "date_published": "2026-09-24T21:05:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "7cd0cff4bf28d65ea726", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioli", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Deano’s Pasta Issue Allergy Alert on Undeclared Lobster in Pear and Pecorino Triangoli Ravioli", "item_type": "entry", "summary": "added: Deano’s Pasta Issue Allergy Alert on Undeclared Lobster in Pear and Pecorino Triangoli Ravioli", "after": { "title": "Deano’s Pasta Issue Allergy Alert on Undeclared Lobster in Pear and Pecorino Triangoli Ravioli", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioli", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioli", "author": "FDA", "published_at": "2026-09-24T21:05:00Z", "updated_at": "2026-09-24T21:05:00Z", "summary": "Deano’s Pasta of Somerville, MA is recalling approximately 20 lbs. of Pear and Pecorino Triangoli Ravioli, because it may contain undeclared Lobster. People who have an allergy or severe sensitivity to Crustacean Shellfish (Lobster) run the risk of serious or life-threatening allergic reaction if th", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioli" }, { "id": "9170973a4b109e17cf28", "title": "Galil Importing Corp Recalls Lior Cinnamon Ground Seasoning Due to Elevated Lead Levels", "content_text": "Galil Importing Corp of Hauppauge, New York is recalling Lior Cinnamon Ground Seasoning because it has the potential to be contaminated with elevated levels of lead. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be t", "date_published": "2026-09-24T20:45:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "9170973a4b109e17cf28", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/galil-importing-corp-recalls-lior-cinnamon-ground-seasoning-due-elevated-lead-levels", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Galil Importing Corp Recalls Lior Cinnamon Ground Seasoning Due to Elevated Lead Levels", "item_type": "entry", "summary": "added: Galil Importing Corp Recalls Lior Cinnamon Ground Seasoning Due to Elevated Lead Levels", "after": { "title": "Galil Importing Corp Recalls Lior Cinnamon Ground Seasoning Due to Elevated Lead Levels", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/galil-importing-corp-recalls-lior-cinnamon-ground-seasoning-due-elevated-lead-levels", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/galil-importing-corp-recalls-lior-cinnamon-ground-seasoning-due-elevated-lead-levels", "author": "FDA", "published_at": "2026-09-24T20:45:00Z", "updated_at": "2026-09-24T20:45:00Z", "summary": "Galil Importing Corp of Hauppauge, New York is recalling Lior Cinnamon Ground Seasoning because it has the potential to be contaminated with elevated levels of lead. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be t", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/galil-importing-corp-recalls-lior-cinnamon-ground-seasoning-due-elevated-lead-levels" }, { "id": "9268aa219450c4724762", "title": "Berlin Seeds Recalls Alfalfa Sprouting Seed Because of Possible Health Risk", "content_text": "Berlin Seeds, of Millersburg, OH, is recalling 950 lbs of Alfalfa Sprouting Seed because the seed has the potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) and/or Salmonella.", "date_published": "2026-09-23T21:02:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "9268aa219450c4724762", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-risk", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Berlin Seeds Recalls Alfalfa Sprouting Seed Because of Possible Health Risk", "item_type": "entry", "summary": "added: Berlin Seeds Recalls Alfalfa Sprouting Seed Because of Possible Health Risk", "after": { "title": "Berlin Seeds Recalls Alfalfa Sprouting Seed Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-risk", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-risk", "author": "FDA", "published_at": "2026-09-23T21:02:00Z", "updated_at": "2026-09-23T21:02:00Z", "summary": "Berlin Seeds, of Millersburg, OH, is recalling 950 lbs of Alfalfa Sprouting Seed because the seed has the potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) and/or Salmonella.", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-risk" }, { "id": "4dcd750a4a62e6157d65", "title": "Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk", "content_text": "Global Mix Inc. of Middle Village, New York, is recalling niwali Tejocote Capsules (90 capsules, Herbal Supplement) and niwali Tejocote Pieces (90 Day Supply, Herbal Supplement) because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of th", "date_published": "2026-09-21T19:40:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "4dcd750a4a62e6157d65", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-niwali-tejocote-capsules-and-niwali-tejocote-pieces-because-possible-health", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk", "item_type": "entry", "summary": "added: Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk", "after": { "title": "Global Mix Inc. Recalls Niwali Tejocote Capsules and Niwali Tejocote Pieces Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-niwali-tejocote-capsules-and-niwali-tejocote-pieces-because-possible-health", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-niwali-tejocote-capsules-and-niwali-tejocote-pieces-because-possible-health", "author": "FDA", "published_at": "2026-09-21T19:40:00Z", "updated_at": "2026-09-21T19:40:00Z", "summary": "Global Mix Inc. of Middle Village, New York, is recalling niwali Tejocote Capsules (90 capsules, Herbal Supplement) and niwali Tejocote Pieces (90 Day Supply, Herbal Supplement) because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of th", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/global-mix-inc-recalls-niwali-tejocote-capsules-and-niwali-tejocote-pieces-because-possible-health" }, { "id": "96d6a4881dfa2e0e01e1", "title": "GF Blends Recalls Truly AIP All Purpose Flour and Bread Mix, and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix Due to Potential Undeclared Wheat Gluten", "content_text": "GF Blends is recalling Truly AIP All Purpose Flour and Bread Mix and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix listed below due to potential undeclared wheat gluten. People who have celiac disease or a severe gluten intolerance run the risk of adverse health effects or allergic reactions if they con", "date_published": "2026-09-18T21:48:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "96d6a4881dfa2e0e01e1", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mix", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "GF Blends Recalls Truly AIP All Purpose Flour and Bread Mix, and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix Due to Potential Undeclared Wheat Gluten", "item_type": "entry", "summary": "added: GF Blends Recalls Truly AIP All Purpose Flour and Bread Mix, and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix Due to Potential Undeclared Wheat Gluten", "after": { "title": "GF Blends Recalls Truly AIP All Purpose Flour and Bread Mix, and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix Due to Potential Undeclared Wheat Gluten", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mix", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mix", "author": "FDA", "published_at": "2026-09-18T21:48:00Z", "updated_at": "2026-09-18T21:48:00Z", "summary": "GF Blends is recalling Truly AIP All Purpose Flour and Bread Mix and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix listed below due to potential undeclared wheat gluten. People who have celiac disease or a severe gluten intolerance run the risk of adverse health effects or allergic reactions if they con", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mix" }, { "id": "0c3757466cfffdc2f3f4", "title": "Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter", "content_text": "ROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose or stopper materia", "date_published": "2026-09-18T19:14:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "0c3757466cfffdc2f3f4", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-dexmedetomidine-hcl-09-sodium-chloride", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter", "item_type": "entry", "summary": "added: Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter", "after": { "title": "Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-dexmedetomidine-hcl-09-sodium-chloride", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-dexmedetomidine-hcl-09-sodium-chloride", "author": "FDA", "published_at": "2026-09-18T19:14:00Z", "updated_at": "2026-09-18T19:14:00Z", "summary": "ROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose or stopper materia", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/par-health-issues-voluntary-nationwide-recall-two-lots-dexmedetomidine-hcl-09-sodium-chloride" }, { "id": "a9ad9590a47c95032782", "title": "Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection", "content_text": "Otsuka ICU Medical LLC is issuing a voluntary recall for one lot of 0.9% SODIUM CHLORIDE Injection, USP, 100mL single pack to the user level due to a potential mix-up. The affected lot of 0.9% SODIUM CHLORIDE Injection, USP (NDC: 0990-7984-23 Lot 1042188) may potentially contain the overwrap with la", "date_published": "2026-09-17T04:00:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "a9ad9590a47c95032782", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/otsuka-icu-medical-llc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-due", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection", "item_type": "entry", "summary": "added: Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection", "after": { "title": "Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/otsuka-icu-medical-llc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-due", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/otsuka-icu-medical-llc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-due", "author": "FDA", "published_at": "2026-09-17T04:00:00Z", "updated_at": "2026-09-17T04:00:00Z", "summary": "Otsuka ICU Medical LLC is issuing a voluntary recall for one lot of 0.9% SODIUM CHLORIDE Injection, USP, 100mL single pack to the user level due to a potential mix-up. The affected lot of 0.9% SODIUM CHLORIDE Injection, USP (NDC: 0990-7984-23 Lot 1042188) may potentially contain the overwrap with la", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/otsuka-icu-medical-llc-issues-voluntary-nationwide-recall-09-sodium-chloride-injection-usp-due" }, { "id": "812d830a22485c5da009", "title": "Saratoga Potato Chips Issues Allergy Alert on Undeclared Soy in J. HIGGS Loaded Bacon and Cheddar Potato Chips", "content_text": "Saratoga Potato Chips of Fort Wayne, IN, is recalling two Best if USED BY codes of 7.75-ounce packages of J. HIGGS Loaded Bacon and Cheddar Potato Chips because they may contain undeclared soy allergen. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threateni", "date_published": "2026-09-16T15:21:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "812d830a22485c5da009", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potato", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Saratoga Potato Chips Issues Allergy Alert on Undeclared Soy in J. HIGGS Loaded Bacon and Cheddar Potato Chips", "item_type": "entry", "summary": "added: Saratoga Potato Chips Issues Allergy Alert on Undeclared Soy in J. HIGGS Loaded Bacon and Cheddar Potato Chips", "after": { "title": "Saratoga Potato Chips Issues Allergy Alert on Undeclared Soy in J. HIGGS Loaded Bacon and Cheddar Potato Chips", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potato", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potato", "author": "FDA", "published_at": "2026-09-16T15:21:00Z", "updated_at": "2026-09-16T15:21:00Z", "summary": "Saratoga Potato Chips of Fort Wayne, IN, is recalling two Best if USED BY codes of 7.75-ounce packages of J. HIGGS Loaded Bacon and Cheddar Potato Chips because they may contain undeclared soy allergen. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threateni", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/saratoga-potato-chips-issues-allergy-alert-undeclared-soy-j-higgs-loaded-bacon-and-cheddar-potato" }, { "id": "b90fa7fbd34138696eab", "title": "So Delicious Dairy Free® Issues Voluntary Recall of Salted Caramel Cluster Non-Dairy Frozen Dessert Pints Due to Potential Presence of Foreign Material", "content_text": "WHITE PLAINS, N.Y. and LOUISVILLE, Colo., September 15, 2026 – Danone USA is issuing a voluntary recall of So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints with best-by dates on and before April 3, 2028 due to the potential presence of foreign materials, such as small", "date_published": "2026-09-15T20:31:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "b90fa7fbd34138696eab", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessert", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "So Delicious Dairy Free® Issues Voluntary Recall of Salted Caramel Cluster Non-Dairy Frozen Dessert Pints Due to Potential Presence of Foreign Material", "item_type": "entry", "summary": "added: So Delicious Dairy Free® Issues Voluntary Recall of Salted Caramel Cluster Non-Dairy Frozen Dessert Pints Due to Potential Presence of Foreign Material", "after": { "title": "So Delicious Dairy Free® Issues Voluntary Recall of Salted Caramel Cluster Non-Dairy Frozen Dessert Pints Due to Potential Presence of Foreign Material", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessert", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessert", "author": "FDA", "published_at": "2026-09-15T20:31:00Z", "updated_at": "2026-09-15T20:31:00Z", "summary": "WHITE PLAINS, N.Y. and LOUISVILLE, Colo., September 15, 2026 – Danone USA is issuing a voluntary recall of So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints with best-by dates on and before April 3, 2028 due to the potential presence of foreign materials, such as small", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessert" }, { "id": "b21f76244ba77b4f8e6e", "title": "Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk", "content_text": "Gias Foods of New York, NY is recalling 2 Lots of bettergoods Authentic Italian Lemon Alfredo Fettuccine, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and ot", "date_published": "2026-09-15T18:52:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "b21f76244ba77b4f8e6e", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk", "item_type": "entry", "summary": "added: Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk", "after": { "title": "Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible", "author": "FDA", "published_at": "2026-09-15T18:52:00Z", "updated_at": "2026-09-15T18:52:00Z", "summary": "Gias Foods of New York, NY is recalling 2 Lots of bettergoods Authentic Italian Lemon Alfredo Fettuccine, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and ot", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible" }, { "id": "dbd4ebb5a0d298727a31", "title": "A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil", "content_text": "Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients ma", "date_published": "2026-09-14T19:55:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "dbd4ebb5a0d298727a31", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-biq-fel-due-undeclared-sildenafil-and-tadalafil", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil", "item_type": "entry", "summary": "added: A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil", "after": { "title": "A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-biq-fel-due-undeclared-sildenafil-and-tadalafil", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-biq-fel-due-undeclared-sildenafil-and-tadalafil", "author": "FDA", "published_at": "2026-09-14T19:55:00Z", "updated_at": "2026-09-14T19:55:00Z", "summary": "Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients ma", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-biq-fel-due-undeclared-sildenafil-and-tadalafil" }, { "id": "95c07ed481b3923a39f9", "title": "A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil", "content_text": "Clermont, Florida – A&P Creations LLC is recalling X10 Natural Enhancement Supplement to the consumer level because it has been found to contain undeclared sildenafil and tadalafil.", "date_published": "2026-09-14T19:06:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "95c07ed481b3923a39f9", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-x10-natural-enhancement-supplement-due-undeclared", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil", "item_type": "entry", "summary": "added: A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil", "after": { "title": "A&P Creations LLC Issues Nationwide Recall of X10 Natural Enhancement Supplement Due to Undeclared Sildenafil and Tadalafil", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-x10-natural-enhancement-supplement-due-undeclared", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-x10-natural-enhancement-supplement-due-undeclared", "author": "FDA", "published_at": "2026-09-14T19:06:00Z", "updated_at": "2026-09-14T19:06:00Z", "summary": "Clermont, Florida – A&P Creations LLC is recalling X10 Natural Enhancement Supplement to the consumer level because it has been found to contain undeclared sildenafil and tadalafil.", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ap-creations-llc-issues-nationwide-recall-x10-natural-enhancement-supplement-due-undeclared" }, { "id": "8d32901e157a18f43558", "title": "Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce", "content_text": "KEASBEY, N.J. (Sept. 14, 2026) –Wakefern Food Corp. has voluntarily recalled select containers of Wholesome Pantry Organic Unsweetened Apple Sauce after routine FDA testing identified elevated patulin levels that exceed food safety limits and do not meet Wakefern's quality standards", "date_published": "2026-09-14T04:00:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "8d32901e157a18f43558", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wakefern-food-corp-voluntarily-recalls-wholesome-pantry-organic-unsweetened-apple-sauce", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce", "item_type": "entry", "summary": "added: Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce", "after": { "title": "Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wakefern-food-corp-voluntarily-recalls-wholesome-pantry-organic-unsweetened-apple-sauce", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wakefern-food-corp-voluntarily-recalls-wholesome-pantry-organic-unsweetened-apple-sauce", "author": "FDA", "published_at": "2026-09-14T04:00:00Z", "updated_at": "2026-09-14T04:00:00Z", "summary": "KEASBEY, N.J. (Sept. 14, 2026) –Wakefern Food Corp. has voluntarily recalled select containers of Wholesome Pantry Organic Unsweetened Apple Sauce after routine FDA testing identified elevated patulin levels that exceed food safety limits and do not meet Wakefern's quality standards", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wakefern-food-corp-voluntarily-recalls-wholesome-pantry-organic-unsweetened-apple-sauce" }, { "id": "cee89e068708859a686d", "title": "Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese", "content_text": "Whole Foods Market of Austin, TX is recalling Fromagerie Coop de Mean Cabricharme cheese because the product contains egg lysozyme, an egg white protein, which is not declared on the product label. People who have an allergy or severe sensitivity to eggs run the risk of a serious or life-threateni", "date_published": "2026-09-11T22:15:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "cee89e068708859a686d", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheese", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese", "item_type": "entry", "summary": "added: Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese", "after": { "title": "Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheese", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheese", "author": "FDA", "published_at": "2026-09-11T22:15:00Z", "updated_at": "2026-09-11T22:15:00Z", "summary": "Whole Foods Market of Austin, TX is recalling Fromagerie Coop de Mean Cabricharme cheese because the product contains egg lysozyme, an egg white protein, which is not declared on the product label. People who have an allergy or severe sensitivity to eggs run the risk of a serious or life-threateni", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheese" }, { "id": "41bd3e9d0c5925bdb745", "title": "Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels", "content_text": "FOR IMMEDIATE RELEASE – 9/9/2026 – Houston, Texas, Centric Compounding is voluntarily recalling 6 lots of Glutathione 200mg/mL, Myer’s Cocktail, and Tri-Immune Boost injectable vials to the consumer level. The products have been found to be compounded with a Glutathione API containing elevated endot", "date_published": "2026-09-11T15:00:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "41bd3e9d0c5925bdb745", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/centric-compounding-issues-nationwide-recall-glutathione-myers-cocktail-and-tri-immune-boost-due", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels", "item_type": "entry", "summary": "added: Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels", "after": { "title": "Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/centric-compounding-issues-nationwide-recall-glutathione-myers-cocktail-and-tri-immune-boost-due", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/centric-compounding-issues-nationwide-recall-glutathione-myers-cocktail-and-tri-immune-boost-due", "author": "FDA", "published_at": "2026-09-11T15:00:00Z", "updated_at": "2026-09-11T15:00:00Z", "summary": "FOR IMMEDIATE RELEASE – 9/9/2026 – Houston, Texas, Centric Compounding is voluntarily recalling 6 lots of Glutathione 200mg/mL, Myer’s Cocktail, and Tri-Immune Boost injectable vials to the consumer level. The products have been found to be compounded with a Glutathione API containing elevated endot", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/centric-compounding-issues-nationwide-recall-glutathione-myers-cocktail-and-tri-immune-boost-due" }, { "id": "a00627e9f0857c719269", "title": "Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk", "content_text": "09/10/2026, Evergreen Fresh Sprouts LLC of Moyie Springs, IDAHO is recalling 215 cases (6/4oz bags per case) of Broccoli Sprouts, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly pe", "date_published": "2026-09-10T20:37:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "a00627e9f0857c719269", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-risk", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk", "item_type": "entry", "summary": "added: Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk", "after": { "title": "Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-risk", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-risk", "author": "FDA", "published_at": "2026-09-10T20:37:00Z", "updated_at": "2026-09-10T20:37:00Z", "summary": "09/10/2026, Evergreen Fresh Sprouts LLC of Moyie Springs, IDAHO is recalling 215 cases (6/4oz bags per case) of Broccoli Sprouts, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly pe", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-risk" }, { "id": "0a00baf15bc125411e37", "title": "FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches", "content_text": "September 4, 2026 Orlando, FL– FreshPoint of Orlando, FL., is issuing a voluntary recall of 1,093 units of specific lots of Cranberry Chicken Salad Wedge sandwiches due to an improperly declared allergen (eggs). People who have an allergy or severe sensitivity to eggs run the risk of serious or lif", "date_published": "2026-09-08T19:31:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "0a00baf15bc125411e37", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwiches", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches", "item_type": "entry", "summary": "added: FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches", "after": { "title": "FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwiches", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwiches", "author": "FDA", "published_at": "2026-09-08T19:31:00Z", "updated_at": "2026-09-08T19:31:00Z", "summary": "September 4, 2026 Orlando, FL– FreshPoint of Orlando, FL., is issuing a voluntary recall of 1,093 units of specific lots of Cranberry Chicken Salad Wedge sandwiches due to an improperly declared allergen (eggs). People who have an allergy or severe sensitivity to eggs run the risk of serious or lif", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwiches" }, { "id": "e1eb9478fa40261d52e1", "title": "BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect", "content_text": "On July 15, 2026, BMC Medical Co., Ltd. (BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. This corrective action was not reported to customers. O", "date_published": "2026-09-07T14:55:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "e1eb9478fa40261d52e1", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bmc-medical-co-ltd-recalls-luna-g3-apap-model-lg3600-firmware-g3-20076-due-firmware-defect", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect", "item_type": "entry", "summary": "added: BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect", "after": { "title": "BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bmc-medical-co-ltd-recalls-luna-g3-apap-model-lg3600-firmware-g3-20076-due-firmware-defect", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bmc-medical-co-ltd-recalls-luna-g3-apap-model-lg3600-firmware-g3-20076-due-firmware-defect", "author": "FDA", "published_at": "2026-09-07T14:55:00Z", "updated_at": "2026-09-07T14:55:00Z", "summary": "On July 15, 2026, BMC Medical Co., Ltd. (BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. This corrective action was not reported to customers. O", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bmc-medical-co-ltd-recalls-luna-g3-apap-model-lg3600-firmware-g3-20076-due-firmware-defect" }, { "id": "3c662ec852a6c138d214", "title": "Made Fresh Salads, Inc. Recalls Ready to Eat Deli Style Salads and Cream Cheese Because of Possible Health Risk", "content_text": "Made Fresh Salads Inc. of Bay Shore, NY is recalling all Ready to Eat Deli Style Salads and cream cheese, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and", "date_published": "2026-09-06T04:00:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "3c662ec852a6c138d214", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-health", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Made Fresh Salads, Inc. Recalls Ready to Eat Deli Style Salads and Cream Cheese Because of Possible Health Risk", "item_type": "entry", "summary": "added: Made Fresh Salads, Inc. Recalls Ready to Eat Deli Style Salads and Cream Cheese Because of Possible Health Risk", "after": { "title": "Made Fresh Salads, Inc. Recalls Ready to Eat Deli Style Salads and Cream Cheese Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-health", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-health", "author": "FDA", "published_at": "2026-09-06T04:00:00Z", "updated_at": "2026-09-06T04:00:00Z", "summary": "Made Fresh Salads Inc. of Bay Shore, NY is recalling all Ready to Eat Deli Style Salads and cream cheese, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-health" }, { "id": "7ccea96f796f280df1a0", "title": "Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk", "content_text": "Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened", "date_published": "2026-09-04T14:19:00Z", "_unlimitedpipe": { "event": { "schema": "unlimitedpipe.event/1", "id": "7ccea96f796f280df1a0", "source": "rss", "type": "change", "key": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-risk", "source_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "timestamp": null, "observed_at": "2026-09-26T00:24:43Z", "data": { "change": "added", "label": "Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk", "item_type": "entry", "summary": "added: Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk", "after": { "title": "Foods Alive Recalls Organic Moringa Leaf Powder Because of Possible Health Risk", "link": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-risk", "id": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-risk", "author": "FDA", "published_at": "2026-09-04T14:19:00Z", "updated_at": "2026-09-04T14:19:00Z", "summary": "Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened", "categories": [], "feed": { "title": "Food and Drugs Administration--Recalls/Safety Alerts", "url": "http://www.fda.gov/", "feed_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml" } } }, "metadata": { "status": 200, "final_url": "https://www.fda.gov/about-fda/contact-fda/stay-informed/rss-feeds/recalls/rss.xml", "elapsed_ms": 83, "not_modified": false, "method": "rss20" }, "provenance": [ { "step": "rss", "version": "0.3.2" }, { "step": "diff", "version": "0.3.2", "args": { "namespace": "food-drug-recalls", "only": [ "added" ], "emit_initial": true } } ] } }, "url": "http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-risk" } ] }