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Recall totals

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

37,326

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/winco-foods-llc-issues-allergy-alert-undeclared-sesame-hoagie-rollsPublished October 22, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 23, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall TerminatedTerminated: June 26, 2023Historical 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 TerminatedTerminated: June 26, 2023Historical 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 TerminatedTerminated: February 27, 2023Historical 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 TerminatedTerminated: June 9, 2022Historical 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 TerminatedTerminated: June 9, 2022Historical 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

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FDA Recall TerminatedTerminated: December 21, 2022Historical recordClass II