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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 14, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray, NET WT 160g (5.6 OZ) can, packaged as (a) single pack, UPC 0 41100 58720 6, NDC 11523-0010-2; (b) 3-pack, UPC 0 41100 58961 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland,

by Bayer Healthcare Pharmaceuticals Inc.

Reason: cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 0 41100 59036 7, NDC 11523-0010-1.

by Bayer Healthcare Pharmaceuticals Inc.

Reason: cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Published: November 24, 2021
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

LOTRIMIN AF (Miconazole nitrate 2%) Powder Spray NET WT 133g (4.6 OZ) can, packaged as (a) a single pack NDC 11523-0544-2 UPC 3 11017 41025 7; (b) 3 pack, NDC 11523-0544-2, UPC 0 41100 58594 3; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, ,

by Bayer Healthcare Pharmaceuticals Inc.

Reason: cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

LOTRIMIN AF (Miconazole nitrate 2%) Jock Itch Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-4140-2. UPC 3 11017 41031 8

by Bayer Healthcare Pharmaceuticals Inc.

Reason: cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3

by Bayer Healthcare Pharmaceuticals Inc.

Reason: cGMP Deviations: manufactured at the same facility where other lots were found to be contaminated with benzene.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clonidine Transdermal System, USP 0.1 mg/day, 4 patches per carton, Rx only, Manufactured by: Actavis Laboratories, UT Inc., Salt Lake City, UT, Distributed by: Actavis Pharma, Inc., Parsippany, NJ NDC 0591-3508-04

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Flocinolone Acetonide 0.01% Topical Oil, Scalp Oil, Rx, packaged in 4 oz. bottle, Distributed by: Amneal Pharmaceuticals Bridgewater, NJ 08807, NDC 65162-703-86

by Amneal Pharmaceuticals of New York, LLC

Reason: Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Flocinolone Acetonide 0.01% Topical Oil, Body Oil, Rx, packaged in 4 oz. bottle, Distributed by: Amneal Pharmaceuticals Bridgewater, NJ 08807, NDC 65162-704-86

by Amneal Pharmaceuticals of New York, LLC

Reason: Subpotent Drug: Out-of-specification assay result was obtained for Fluocinolone Acetonide.
Published: November 24, 2021
Distribution: Nationwide

View recall →

FDA Recall Terminated Historical recordClass II