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

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Source: FDA and USDA public dataLast updated September 13, 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

Rufinamide Tablets, USP 200 mg, packaged in 120-count bottle, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India, NDC 59651-616-08

by Aurobindo Pharma USA Inc.

Reason: cGMP deviations: Batch was released prior to approval.
Published: August 30, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Real Kosher Ice Cream, Inc.

Product: Soft Zero on the Go brand Lite Peanut Butter flavor; 8 fl oz…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: August 30, 2023
Distribution: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass I

Real Kosher Ice Cream, Inc.

Product: Soft Serve on the Go brand Sorbet Strawberry Mango Sorbet fl…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: August 30, 2023
Distribution: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass I

Real Kosher Ice Cream, Inc.

Product: Soft Serve on the Go brand Caramel Vanilla flavor; 8 fl oz;…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: August 30, 2023
Distribution: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass I

Real Kosher Ice Cream, Inc.

Product: Soft Serve on the Go brand Razzle n' Dazzle Peanut Butter fl…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: August 30, 2023
Distribution: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass I

Real Kosher Ice Cream, Inc.

Product: Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz…
Reason: Product may be contaminated with Listeria monocytogenes.
Published: August 30, 2023
Distribution: CA, CO, CT, DC, DE, FL, IL, MA, MD, MI,…

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FDA Recall United States Terminated Historical recordClass II

Bickel's Snack Foods Inc

Product: Butter Flavored Popcorn Naturally & Artificially Flavored, 8…
Reason: Undeclared milk
Published: August 30, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Inmar Supply Chain Solutions, LLC

Product: Multiple FDA-regulated products. Pallets
Reason: Potential exposure to rodents and rodent activity in the warehouse.
Published: August 30, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Tobramycin Opthalmic Solution USP, 0.3%, 5mL bottle, Rx only, Manufactured for: Alembic Pharmaceuticals, Bedminster, NJ 07921, USA, NDC 62332-518-05

by ALEMBIC PHARMACEUTICALS, INC.

Reason: Failed Impurities/Degradation Specifications
Published: August 23, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61

by Advanced Accelerator Applications USA, Inc.

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date
Published: August 23, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II