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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.

37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2
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Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 14,161–14,180 of 23,259 recalls

FDA Recall United States Terminated Historical recordClass II

Ziegenfelder Company, Inc.

Product
Budget $aver Monster Cherry-Pineapple Pops Net Contents 36 F…
Reason
The Colorado Department of Public Health & Environment notified the firm that they had recovered Listeria monocytogenes from multiple environmental sampling sites collected during an inspection at their Denver plant.
Published
May 16, 2018
Distribution
Product distributed to retail stores and…

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FDA Recall United States Terminated Historical recordClass II

Ziegenfelder Company, Inc.

Product
Budget $aver Sugar Free Twin Pops Net Contents 28.2 FL OZ
Reason
The Colorado Department of Public Health & Environment notified the firm that they had recovered Listeria monocytogenes from multiple environmental sampling sites collected during an inspection at their Denver plant.
Published
May 16, 2018
Distribution
Product distributed to retail stores and…

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FDA Recall United States Terminated Historical recordClass III

Sugarfina, LLC

Product
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC:…
Reason
Internal audit discovered that their Platinum Bling Ring product contains fish gelatin that is not declared on the ingredient or allergen information
Published
May 16, 2018
Distribution
FL, AR, OR, UT, PA, CA, NJ, MA,NY, MD, I…

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FDA Recall United States Terminated Historical recordClass II

MUNK PACK INC

Product
Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT…
Reason
Mold growth on product.
Published
May 16, 2018
Distribution
CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,N…

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FDA Recall United States Terminated Historical recordClass II

MUNK PACK INC

Product
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz…
Reason
Mold growth on product.
Published
May 16, 2018
Distribution
CA,CO,CT,FL,GA,IA,IL,IN,MA,MD,MS,NH,NJ,N…

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FDA Recall United States Terminated Historical recordClass II

NatureBox, Inc.

Product
Whole Wheat Chocolate Animal Cookies; 5 oz. pouch, 5 lb. Co…
Reason
While packing from a bulk bin of whole wheat chocolate animal cookies, 2 whole wheat vanilla animal cookies were discovered. The vanilla cookies contain soy lecithin that is not declared on the chocolate cookie label.
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Cookies & Cream 1,000g (2.2lb) Tub
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Chocolate 2,268g (5lb) Tub and Lean Pro 8 Chocola…
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Labrada Nutrition, Inc

Product
Lean Pro 8 Vanilla 2,268g (5lb) Tub
Reason
Undeclared egg
Published
May 16, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bob's Red Mill Natural Foods, Inc.

Product
Bob's Red Mill 100% Whole Wheat Bread Mix, Item 1674C194, pa…
Reason
100% Whole Wheat Bread Mix is recalled due to undeclared wheat in the label on the back side of the package.
Published
May 16, 2018
Distribution
Distributed in CA, IL, FL, MI, NH, NJ, N…

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FDA Recall Terminated Historical recordClass II

Docetaxel injection concentrate, 20 mg/mL, 1 mL vial, Rx only, Winthrop U.S. a business of Sanofi-Aventis U.S. LLC., NDC 0955-1020-01

by Sanofi-Aventis U.S. LLC

Reason
Superpotent drug: over-concentrated vials of Docetaxel injection concentrate 20 mg/mL may have been distributed.
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only 90-count bottle. Marketed by: Rhodes Pharmaceuticals L.P., Coventry, RI 02816. Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834. NDC 42858-402-45

by Rhodes Pharmaceuticals, L.P.

Reason
Failed Dissolution Specification: Low dissolution outside of specifications
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 750 mg Levofloxacin (5 mg/mL) in 150 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-245-52

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 500 mg Levofloxacin (5 mg/mL) in 100 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-244-47

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levetiracetam in 0.54% Sodium Chloride Injection, 1,500 mg per 100 mL (15 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-248-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levetiracetam in 0.75% Sodium Chloride Injection, 1000 mg per 100 mL (10 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-247-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levetiracetam in 0.82% Sodium Chloride Injection, 500 mg per 100 mL (5 mg/mL), For Intravenous Infusion Only, Distributed By: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-246-47.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for: AuroMedics Pharma, LLC, NDC 55150-243-46.

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Linezolid Injection 600 mg per 300 mL (2 mg/mL) For Intravenous Administration, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for AuroMedics Pharma, LLC, NDC 55150-242-51

by AuroMedics Pharma LLC

Reason
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyn…
Reason
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

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Data last updated:

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.