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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 November 2026.

37,450
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ready-foods-llc-recalls-fresh-you-brand-sausage-egg-cheese-biscuit-sandwich-due-possiblePublished November 8, 2026
Most affected stateHawaii 200 recalls mention this state

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Download matching recalls as CSV

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 15,321–15,340 of 21,307 recalls

FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/325 mg per 15 mL C-II, a) 4 fl.oz .(120 mL), 12 bottles per case (NDC 66689-023-04), b) 16 fl.oz. (473 mL), 12 bottles per case (NDC 66689-023-16), c) 50 unit dose cups of 15 mL per case, (NDC No. 66689-023-50), Rx only, Manufactured by VistaPharm, Largo, FL 33771

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 26, 2021Historical recordClass II

Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 bottles per case (NDC 66689-008-02), b) 16 fl. oz. (237 mL), 12 bottles per case (NDC 66689-008-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall TerminatedTerminated: June 22, 2018Historical 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 TerminatedTerminated: June 29, 2018Historical 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 TerminatedTerminated: October 19, 2017Historical 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 TerminatedTerminated: October 19, 2017Historical 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 TerminatedTerminated: October 19, 2017Historical 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 TerminatedTerminated: October 19, 2017Historical 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 TerminatedTerminated: June 22, 2018Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical 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 TerminatedTerminated: March 1, 2017Historical recordClass I

Houdini Inc.

Product
Alfasi Cabernet Kosher Selection Basket #810
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 1, 2017Historical recordClass I

Houdini Inc.

Product
Houdini Napa Valley Collection Basket #766
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 1, 2017Historical recordClass I

Houdini Inc.

Product
Vintners Path Cabernet Seasons Greetings Basket #763
Reason
Potential Salmonella contamination.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 1, 2017Historical recordClass I

Houdini Inc.

Product
Stags Leap Winery Collection Basket #752
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.

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