Data Explorer

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 November 2026.

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 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 November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: May 30, 2018Historical recordClass II

Riomet (metformin hydrochloride) Oral Solution Cherry Flavored 500 mg /5 mL, 4 fl. oz. (NDC 10631-206-01) and 16 fl. oz. (NDC 10631-206-02) HDPE bottles, Rx only, Manufactured for: Ranbaxy Laboratories Inc. Jacksonville, FL 32257 USA, Distributed by: Sun Pharmaceutical Industries, Cranbury, NJ 08512

by Sun Pharmaceutical Industries, Inc.

Reason: Microbial Contamination of Non-Sterile Products
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 3, 2018Historical recordClass III

Penicillin V Potassium for Oral Solution, USP, 125 mg (200,000 U) per 5 mL, 100 mL (when mixed) bottle, Rx only, Manufactured In Canada By: Teva Canada Limited, Toronto, Canada M1B 2K9; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454; NDC 0093-4125-73.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Published: December 20, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: January 23, 2018Historical recordClass I

Wang Globalnet

Product: Fish Cake in Polybag 10/930g, Item no. 15731 UPC Code 08770…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States TerminatedTerminated: January 23, 2018Historical recordClass I

Wang Globalnet

Product: Fish Cake in Polybag 10/2.2lbs, Item no. 12842 UPC Code 087…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States TerminatedTerminated: January 23, 2018Historical recordClass I

Wang Globalnet

Product: Fish Tofu in Polybag 40/240g, Item no. 17185, UPC Code 08770…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States TerminatedTerminated: January 23, 2018Historical recordClass I

Wang Globalnet

Product: Fish Ball in Polybag 24/12oz., Item no. 20072, UPC Code 0877…
Reason: Fish products contain undeclared egg and wheat.
Published: December 20, 2017
Distribution: NY, NJ, PA, MA, ME, VA, MD, DE, CT, RI,…

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FDA Recall United States TerminatedTerminated: January 23, 2018Historical recordClass I