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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: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 24, 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 United States TerminatedTerminated: November 3, 2022Historical recordClass I

Keswick Creamery at Carrock Farms LLC

Product: Aged raw milk cheese "Wallaby" 4 oz to 12 oz packages
Reason: All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Distributed to farm stores and farmers m…

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FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Keswick Creamery at Carrock Farms LLC

Product: Aged raw milk cheese "Vulkwin's Folly Scratch 2" 4oz-12oz pa…
Reason: All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Distributed to farm stores and farmers m…

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FDA Recall United States TerminatedTerminated: November 3, 2022Historical recordClass I

Keswick Creamery at Carrock Farms LLC

Product: Aged raw milk cheese "Ploughman Cider Wash Tomme" batch 47 4…
Reason: All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Distributed to farm stores and farmers m…

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FDA Recall United States TerminatedTerminated: October 28, 2022Historical recordClass II

Beverage Distribution Center Incorporated, LLC. (BDCI)

Product: "A&W Root Beer Zero Sugar" packaged in 20oz PET bottles. UPC…
Reason: Product contains undeclared sugar. Full sugar root beer was packaged in bottles labeled "sugar free"
Published: October 5, 2022
Distribution: Distributed in Washington DC, MD, PA, an…

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FDA Recall TerminatedTerminated: March 2, 2023Historical recordClass III

Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC. East Brunswick, NJ 08816. NDC# 29300-137-01

by UNICHEM PHARMACEUTICALS USA INC

Reason: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Published: September 28, 2022
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 21, 2023Historical recordClass III

Pepsico Inc

Product: Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as…
Reason: The outer wraps match the liquid in the can (Zero Sugar - Mountain Dew Major Melon) however the primary package (can) is incorrect (Full Sugar Mountain Dew Major Melon). Product inside can matches the product/nutritional panel on the point-of-sale outer container wrap.
Published: September 28, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 30, 2025Historical recordClass I

PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA

by Pfizer Inc.

Reason: Presence of particulate matter
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: August 14, 2023Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, Rx Only, 100 tablets per bottle, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0555-0777-02.

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 27, 2023Historical recordClass II

Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.

by SUPERIOR GLOVE WORKS, LTD.

Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 31, 2024Historical recordClass II