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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.

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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)

  • 1,527 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

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

Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,561–12,580 of 17,335 recalls

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-887-32; Blister NDC 68084-887-33

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 25 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-909-32; Blister NDC 68084-909-33

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-832-25; Blister NDC 68084-832-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 15 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-898-32; Blister NDC 68084-898-33

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 10 mg 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-815-25; Blister NDC 68084-815-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 30 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 60687-154-25; Blister NDC 60687-154-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 20 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-943-25; Blister NDC 68084-943-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 15 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 60687-133-25; Blister NDC 60687-133-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 10 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-936-25; Blister NDC 68084-936-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-874-25; Blister NDC 68084-874-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection, 10 mL multidose vial, sterile. Rx only. Compounded by Isomeric Pharmacy Solutions, Salt Lake City, UT 84109,

by Isomeric Pharmacy Solution, LLC

Reason
Lack of Processing Controls: Isomeric Pharmacy Solution, LLC announces a voluntary field action for the Methylprednisolone Acetate/Lidocaine HCl 40/10 mg/mL Injection because the sterile injectable products were sterilized too long leading to potential difficulty resuspending particles.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) adult gummies Multi for Her plus Omega-3, 150…
Reason
Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

McCain Foods USA

Product
Fire roasted Poblano & Jalapeno popper bites packaged in a w…
Reason
Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) D3 1000IU, 350 count, UPC 0-31604-04070-3
Reason
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

Geneva Foods, LLC

Product
Lysander's All Natural Bourbon Flavor Rub; for beef, chicken…
Reason
Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) Multi + Omega-3, 150 count, UPC 0-31604-04173…
Reason
Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC…
Reason
Specific lots of Nature Made(R) adult gummies Hair.Skin.Nails may exceed specifications total viable plate count.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
Reason
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

McCain Foods USA

Product
Breaded stuffed Jalapenos poppers labeled in part: Anchor br…
Reason
Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) adult gummies Multi, 90 count, UPC 0-31604-02…
Reason
Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published
September 14, 2016
Distribution
Nationwide

View recall →

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.