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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,118

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://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-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

State: AS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 19, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Completed Historical recordClass II

Camber Pharmaceuticals, Inc. Valsartan Tablets, USP, 80 mg, 90 count bottles, Rx Only Manufactured for: Camber Pharmaceuticals, Inc. Piscataway NJ 08854 By: Hetero Hetero Labs Limited Unit V. Polepally Jadcherla Mahaboob Nagar - 509-301 India. NDC 31722-746-90 UPC 331722746908

by Hetero Labs Limited Unit V

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Camber Pharmaceuticals, Inc. Valsartan Tablets, USP, 40 mg, 30 Tablets Rx Only Manufactured for: Camber Pharmaceuticals, Inc. Piscataway NJ 08854 By: Hetero Hetero Labs Limited Unit V, Polepally Jadcherla Mahaboob Nagar - 509-301, India. NDC 31722-745-30 UPC 331722745307

by Hetero Labs Limited Unit V

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Diltiazem HCl Extended-release Capsules, USP 120 mg, 80 capsules, 8 blister cards of 10 capsules each per carton, Rx Only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV. NDC 51079-947-08

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Impurities/Degradation Specifications; out of specification results for related compound per the manufacturer
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide Tablets, Valsartan 320 MG and Hydrochlorothiazide 25 MG, 90 tablets per bottle, Rx Only, MFG: Arrow Pharm (Malta) LTD, Birzebbugia, BBG 3000 Malta. NDC: 54569-6488-0

by A-S Medication Solutions LLC.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide Tablets, Valsartan 160 MG and Hydrochlorothiazide 12.5 MG, 90 tablets per bottle, Rx Only, MFG: Arrow Pharm (Malta) LTD, Birzebbugia, BBG 3000 Malta. NDC: 54569-6480-0

by A-S Medication Solutions LLC.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, 80 MG, 30-count bottle (NDC 54569-6582-0, 90-count bottle (NDC 54569-6582-1), Rx Only, MFG: Zhejiang Huahai Pharma, Linhai, Zhejiang 317024 China

by A-S Medication Solutions LLC.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, 160 MG, 30-count bottle (NDC 54569-6583-0), 90-count bottle (NDC 54569-6583-1), Rx Only, MFG: Zhejiang Huahai Pharma, Linhai, Zhejiang 317024 China

by A-S Medication Solutions LLC.

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Country Favor Inc.

Product: BEST TASTE BRAND SNACK GINGER SLICED, Net Weight 200g, 7 OZ,…
Reason: Product contains high levels of undeclared sulfites.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Gift Services Inc Warehouse

Product: Sherman Candy Caramels are individually wrapped in plastic a…
Reason: Sherman Candy Caramels product is recalled due to undeclared pecans, walnuts, almonds and/or peanuts.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Natures Bounty Inc

Product: BLUE GREEN ALGAE: Packaged under the following brands: AMERI…
Reason: High level of microcystin observed in the product.
Published: August 29, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets, 8 mg/90 mg, 120-count bottle, Rx only, Distributed by Orexigen therapeutics, Inc., La Jolla, CA 92037, NDC 51267-890-99.

by Orexigen Therapeutics, Inc.

Reason: Defective Container: Customer complaints of punctures in the bottle.
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium tablets, 40 mg, 500-count bottle, Rx only, Mfd By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 India, NDC 55111-123-05

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications - OOS was observed for ATV Cyclo FP Impurity and Total Degradation Impurities tested at the 18 month stability time point in Atorvastatin Calcium Tablets 40 mg 500 tablets.
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Confidence Inc./Confidence U.S.A. Inc.

Product: FP0391 Confidence, Glucosamine Plus, With Hyaluronic Acid +…
Reason: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin.
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Confidence Inc./Confidence U.S.A. Inc.

Product: FP0692, Confidence, Prenatal Multi-V + DHA, 90 tablets per b…
Reason: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol (PEG), Triacetin, FD&C Yellow #6 (Sunset Yellow FCF), FD&C Red #40 (Allura Red AC), FD&C Yellow #5 (Tartrazine), and FD&C Blue #2 (Indigotine).
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Confidence Inc./Confidence U.S.A. Inc.

Product: FP0292 Confidence Nitro-Cross 60s, UPC# 8 92483 00155 7
Reason: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Confidence Inc./Confidence U.S.A. Inc.

Product: FP0392, Confidence, Glucosamine Plus, with White Willow Bark…
Reason: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose (HPMC), Titanium Dioxide, Polyethylene Glycol 400 and 800 (PEG), Triacetin
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Saratoga Food Specialties, Inc.

Product: Pizza Hut Seasoning Breadstick 10 pound case, 5 X 2 lb. pa…
Reason: Saratoga Food Specialties, has initiated a voluntary recall of Pizza Hut Seasonings following their supplier's recall of dry whey powder due to the potential presence of Salmonella
Published: August 22, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Blissful Remedies Gold Series Ultra Enhanced Indo, 50 capsule, packaged in While Foil Pouch, Dist. by World Organix LLC, Las Vegas Nevada UPC# 6 02401 88900 2

by World Organix, LLC

Reason: Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
Published: August 15, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Blissful Remedies Kratom+CBD CBD infused Maeng Da, capsules 50-count packaged in While Foil Pouch. Dist. by World Organix LLC, Las Vegas Nevada UPC# 7 11583 27057 4

by World Organix, LLC

Reason: Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
Published: August 15, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, 12mL bottle. Distributed by World Organix LLC Las Vegas Nevada. UPC#7 14983 56525 7

by World Organix, LLC

Reason: Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.
Published: August 15, 2018
Distribution: Nationwide

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Data last updated: September 19, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.