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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.

37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 10,741–10,760 of 17,327 recalls

FDA Recall Terminated Historical recordClass III

Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per Bottle, Rx only, Distributed By: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5721-56

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Buprenorphine and Naloxone Sublingual Tablets, 2 mg/0.5 mg 30 tablets per bottle, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-5720-56

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: out of specification test results for related compounds largest unknown impurity.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981

by Shionogi Inc.

Reason
Failed Dissolution Specifications: Low dissolution results were obtained during stability testing
Published
July 26, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981, NDC 66993-070-30

by Shionogi Inc.

Reason
Failed Dissolution Specifications: Low dissolution results were obtained during stability testing
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 5 mL Single-use vial, Rx Only, Sterile, Manufactured by: Gland Pharma Limited, Hyderabad, India, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 --- NDC 0409-1140-01

by Hospira Inc., A Pfizer Company

Reason
Failed Impurities/Degradation Specifications; out of specification result for denitroquinoline-related impurity during three month time point
Published
July 26, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B99187, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B94797, BREADER X1@, NET WT 40 LBS, Manufactured By: Newly W…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B94412, BREADER X1@, NET WT 50 LBS, Manufactured By: Newly W…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B94128, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B94110, BREADER X1, NET WT 50 LBS, Manufactured By: Newly We…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B94109, BREADER X1@, NET WT 50 LBS, Manufactured By: Newly W…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B93836, BREADER X1, NET WT 25 LBS, Manufactured By: Newly We…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B93709, BREADER X1@, NET WT 40 LBS, Manufactured By: Newly W…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B93706, BREADER X5, NET WT 50 LBS, Manufactured By: Newly We…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B92659, BREADER X1@, NET WT 35 LBS, Manufactured By: Newly W…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B89414, BATTER MX X1@, NET WT 50 LBS, Manufactured By: Newly…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B89223, BATTER MX X1@, NET WT 50 LBS, Manufactured By: Newly…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B88991, BATTER MX X1@, NET WT 20 LBS, Manufactured By: Newly…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B86031, BATTER MX X1*, NET WT 50 LBS, Manufactured By: Newly…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product
B84127, BATTER MIX X1, NET WT 50 LBS, Manufactured By: Newly…
Reason
Product may contain undeclared milk.
Published
July 26, 2017
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.