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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 9,881–9,900 of 18,116 recalls

FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Low Sodium Brown Gravy Mix 12 oz unit, 8 units per carton…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Beef Flavored Gravy Mix 12 oz unit, 8 units per carton Ite…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Brown Gravy Mix 16 oz unit, 24 units per carton Item 10000…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Queso Snack Seasoning 25 pound bag, 1 bags per carton Item…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Milk and Egg Mix 12 oz bag, 32 bags per carton Item 10000…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Dry Milk and Egg Mix 12 oz bag, 24 bags per carton Item 9…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Griffith Labs U.S.A.

Product
Biscuit Mix 4.5 pound bag, 8 bags per carton Item 12704230…
Reason
Potential presence of Salmonella due to use of recalled whey ingredient
Published
August 8, 2018
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

General Mills, Inc

Product
Cheerios Protein Oats & Honey, Packaged in the following siz…
Reason
Cheerios Protein Oats and Honey cereal may be contaminated with Salmonella.
Published
August 8, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

LL'S MAGNETIC CLAY INC

Product
Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastro…
Reason
The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Published
August 8, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30

by Aidarex Pharmaceuticals LLC

Reason
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published
August 1, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-90

by Aidarex Pharmaceuticals LLC

Reason
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published
August 1, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 2.5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0977-90

by Aidarex Pharmaceuticals LLC

Reason
Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published
August 1, 2018
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, USP 320 mg, 90-count bottle (NDC 0591-2170-19), 500-count bottle (NDC 0591-2170-05), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

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FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, USP 160 mg, 90-count bottle (NDC 0591-2169-19), 1000-count bottle (NDC 0591-2169-10), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

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FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, USP 80 mg, 90-count bottle (NDC 0591-2168-19), 1000-count bottle (NDC 0591-2168-10), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Ongoing Historical recordClass II

Valsartan Tablets, USP 40 mg, 30-count bottle (NDC 0591-2167-30), 90-count bottle (NDC 0591-2167-19), Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/25 mg tablets, USP, 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2318-19.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 320 mg/12.5 mg tablets, USP, 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2318-19

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/25 mg tablets, USP 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2317-19.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

FDA Recall Ongoing Historical recordClass II

Valsartan and Hydrochlorothiazide (HCTZ) Tablets, USP 160 mg/12.5 mg tablets, USP 90-count bottle, Rx Only, Rx Only, Manufactured by: Arrow Pharma (Malta) Ltd. India, Distributed by: Actavis Pharma, Inc. Parsippany, NJ 07054. NDC 0591-2316-19.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published
August 1, 2018
Distribution
Product was distributed throughout the U…

View recall →

Data last updated:

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.