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Recall totals

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

37,327

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 recallhttps://www.fsis.usda.gov/recalls-alerts/imperio-distribution-llc-recalls-beef-jerky-products-produced-without-benefitPublished October 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 25, 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

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

Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can, Labeled as (a) Product of Ireland 86940418, (b)Product of Finland 20006106, (c) Product of Ireland with Instant redeemable coupon ( IRC); Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 3 11017 41009 7, NDC 11523-0777-2.

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 TerminatedTerminated: June 26, 2023Historical recordClass II

Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g (4.6 oz) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Ireland 86951967, UPC 3 11017 41007 3, NDC 11523-0072-5

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 TerminatedTerminated: June 26, 2023Historical recordClass II

Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, labeled as (a) Product of Finland 20006101, (b) Product of Ireland 87022897, (c) Product of Ireland 87022897, with an instant redeemable coupon (IRC) tag attached to the can; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, UPC 3 11017 41005 9, NDC 11523-0165-3 Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can, Labeled as (a) Product of Finland 20006101, (b) Product of Ireland 87022897, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, UPC 3 11017 41005 9, NDC 11523-0165-3.

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

View recall →

FDA Recall TerminatedTerminated: June 26, 2023Historical recordClass II

Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can, labeled as (a) UPC 3 11017-410-00 4, NDC 11523-4162-1, Product of Finland 86568411; (b) UPC 3 11017 41000 4, NDC 11523-4162-1, Product of Finland 20006105; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981

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 TerminatedTerminated: June 26, 2023Historical recordClass II

Lotrimin AF (Miconazole nitrate 2%) Liquid Spray NET WT 133g (4.6 oz) can, Packaged as (a) single pack, UPC 0 41100 40788 7, NDC 11523-4327-1; (b) 3-pack UPC 0 41100 58593 6; 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

View recall →

FDA Recall TerminatedTerminated: June 26, 2023Historical 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

View recall →

FDA Recall TerminatedTerminated: June 26, 2023Historical 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 TerminatedTerminated: June 26, 2023Historical 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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

FDA Recall TerminatedTerminated: December 21, 2022Historical recordClass II

Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules, USP) 120 mg, Rx Only, 90 capsules, labelled as (a) Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054; (b) Manufactured By: Actavis Laboratories FL. Inc, Fort Lauderdale FL. 33314 USA, Distributed by Avista Pharma Inc. Parsippany, NJ 07054 USA. NDC 62037-597-90

by Teva Pharmaceuticals USA

Reason: Labelling: Incorrect Exp. Date
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: November 22, 2021Historical recordClass I

Dole Fresh Vegetables Inc

Product: Salad Classics Garden Salad; iceberg lettuce, shredded carro…
Reason: The Georgia Department of Agriculture sampled and found Listeria monocytogenes in Dole Garden Salad. Product was packed under 3 additional brand names.
Published: November 24, 2021
Distribution: Multiple states

View recall →

FDA Recall United States TerminatedTerminated: November 22, 2021Historical recordClass I

Dole Fresh Vegetables Inc

Product: Kroger Garden Salad; iceberg lettuce, shredded carrots, red…
Reason: The Georgia Department of Agriculture sampled and found Listeria monocytogenes in Dole Garden Salad. Product was packed under 3 additional brand names.
Published: November 24, 2021
Distribution: Multiple states

View recall →

FDA Recall United States TerminatedTerminated: November 22, 2021Historical recordClass I

Dole Fresh Vegetables Inc

Product: Marketside Classic Salad; Garden Salad; iceberg lettuce, shr…
Reason: The Georgia Department of Agriculture sampled and found Listeria monocytogenes in Dole Garden Salad. Product was packed under 3 additional brand names.
Published: November 24, 2021
Distribution: Multiple states

View recall →

FDA Recall United States TerminatedTerminated: November 22, 2021Historical recordClass I

Dole Fresh Vegetables Inc

Product: Dole Garden Salad; iceberg lettuce, shredded carrots, red ca…
Reason: The Georgia Department of Agriculture sampled and found Listeria monocytogenes in Dole Garden Salad. Product was packed under 3 additional brand names.
Published: November 24, 2021
Distribution: Multiple states

View recall →

FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: EveryPlate Meal Kit Product Codes 82-83-89-93-94-96-98 from…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: EveryPlate Meal Kit Product Codes 87-88-89-90-91-94-101 from…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

View recall →

Data last updated: October 25, 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.