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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026
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 11,721–11,740 of 17,335 recalls

FDA Recall Terminated Historical recordClass II

MIDAZOLAM INJECTION, USP, *25 mg/5 mL, (5 mg/ mL), 5 mL vials, 10 Vials per carton, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- NDC 63323-412-05

by Fresenius Kabi USA, LLC

Reason
Failed Impurities/Degradation Specifications
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sun Pharma Carbidopa and Levodopa Tablets USP 25 mg/250 mg a) 100-count bottles (NDC 62756-519-88), b) 500-count bottles (NDC 62756-519-13) Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd. Halol-Baroda Highway, Halol-389 350 Gujarat, India.

by Sun Pharmaceutical Industries, Inc.

Reason
Failed Dissolution Specifications
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Flucanozole Tablets, USP, 200 mg, a) 30 count (NDC 55111-146-30) and b) 100 count (NDC 55111-146-01) bottles, Rx Only, Mfd. by: Dr. Reddy's Laboratories, Bachupally 500 090 India

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications; 18 month stability time point
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Flucanozole Tablets, USP, 150 mg, 12x1 Blister cards, Rx Only, Mfd. by: Dr. Reddy's Laboratories, Bachupally 500 090 India --- NDC 55111-145-12

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications; 18 month stability time point
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Flucanozole Tablets, USP, 100 mg, a) 30 count (NDC 55111-144-30) and b) 100 count (NDC 55111-144-01) bottles, Rx Only, Mfd. by: Dr. Reddy's Laboratories, Bachupally 500 090 India

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications; 18 month stability time point
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Flucanozole Tablets, USP, 50 mg, a) 30 count (NDC 55111-143-30) and b) 100 count (NDC 55111-143-01) bottles, Rx Only, Mfd. by: Dr. Reddy's Laboratories, Bachupally 500 090 India

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications; 18 month stability time point
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Roland Foods, LLC.

Product
Roland MANZANILLA OLIVES STUFFED WITH ANCHOVIES, DR. WT. 3 O…
Reason
Product quality issue. Through sampling, FDA revealed the presence of non-pathogenic Gram Positive Rods (microorganisms).
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Nepro Mixed Berry, 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Vital High Protein, 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Nepro Vanilla , 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Nepro Vanilla High Protein , 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Oxepa, 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass II

Abbott Nutrition

Product
Promote with Fiber Vanilla, 8oz metal can
Reason
The firm expanded recall to include additional batches. Product recalled because of off odor and taste due to microbial contamination.
Published
February 8, 2017
Distribution
The product was distributed in the US as…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Burgundy and Bronze Metal Basket
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
The Classic Basket #6013
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
California Wine Crate Basket #990
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Napa and Sonoma Duet Basket #973
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Alfasi Chardonnay Kosher Selection Basket #847
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Alfasi Kosher Trio Basket #812
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Alfasi Cabernet Kosher Selection Basket #810
Reason
Potential Salmonella contamination.
Published
February 8, 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.