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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.

37,449
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 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 11,841–11,860 of 21,307 recalls

FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
ASK Foods Inc. Naturally Creative Firecracker Slaw, 3.75 lb.…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
ASK Foods Inc. Naturally Creative, Roasted Corn and Edamame…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
ASK Foods Inc. Rigatoni Casserole, 5 lb. Aluminum Tray Pan s…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
ASK Foods Inc. Smokey Mozzarella Pasta Salad, 4 lb. Bulk Co…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
Taste of Inspirations Rotini Salad, Net Wt. 13 oz., Pre-pack…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: December 20, 2018Historical recordClass II

ASK Foods Inc

Product
Wegmans Roasted Corn and Bean Salad; 13 oz. Plastic Contain…
Reason
Products recalled due to potential contamination with Listeria monocytogenes or Salmonella.
Published
December 26, 2018
Distribution
Product Distributed in the following Sta…

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FDA Recall United States TerminatedTerminated: March 11, 2019Historical recordClass I

DANONE WATERS OF AMERICA INC

Product
LIGHT & FIT¿ GREEK CRUNCH NONFAT YOGURT & TOPPINGS S MORES F…
Reason
Danone North America is voluntarily recalling Light & Fit¿ Greek Crunch Nonfat Yogurt & Toppings S Mores Flavor because it was discovered that some of the toppers sold on the product contain peanuts and are improperly labeled.
Published
December 26, 2018
Distribution
13 states: Connecticut, Illinois, Iowa,…

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FDA Recall United States TerminatedTerminated: February 14, 2019Historical recordClass I

Country Favor Inc.

Product
Best Taste Brand DRIED BAMBOO SHOOT Mang Non. The product co…
Reason
Product contains undeclared sulfites (75 mg per serving).
Published
December 26, 2018
Distribution
AL, AR , FL, GA, IL,KY, LA, MA, MD,MI,MO…

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FDA Recall OngoingHistorical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/320 mg/25 mg, (a) 30-count bottles (NDC 0093-7809-56) & 90-count bottles (NDC 0093-7809-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/160 mg/25 mg, (a) 30-count bottles (NDC 0093-7960-56) & 90-count bottles (NDC 0093-7690-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 10 mg/160 mg/12.5 mg, (a) 30-count bottles (NDC 0093-7810-56) & 90-count bottles (NDC 0093-7810-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Amlodipine, Valsartan, and Hydrochlorothiazide Tablets 5 mg/160 mg/12.5 mg, (a) 30-count bottles (NDC 0093-7807-56) & 90-count bottles (NDC 0093-7807-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles (NDC 0093-7693-56) & 90-count bottles (NDC 0093-7693-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets 5 mg/320 mg, (a) 30-count bottles (NDC 0093-7692-56) & 90-count bottles (NDC 0093-7692-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets 10 mg/160 mg, (a) 30-count bottles (NDC 0093-7961-56) & 90-count bottles (NDC 0093-7691-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Amlodipine and Valsartan Tablets 5 mg/160 mg, (a) 30-count bottles (NDC 0093-7690-56) & 90-count bottles (NDC 0093-7690-98), RX Only, Manufactured In Israel By: TEVA PHARMACEUTICAL IND. LTD. Jerusalem, 9777402, Israel, Manufactured For: TEVA PHARMACEUTICALS USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
CGMP Deviations: FDA laboratory testing confirmed presence of an impurity, N-nitrosodimethylamine (NDEA) in product.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 26, 2021Historical recordClass II

Westminster Irbesartan Tablets, USP 300 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-121-01; b) 90 count bottle NDC 69367-121-03

by Westminster Pharmaceuticals LLC

Reason
CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in specific lots of Irbesartan.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 26, 2021Historical recordClass II

Westminster Irbesartan Tablets, USP 150 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-120-01; b) 90 count bottle NDC 69367-120-03

by Westminster Pharmaceuticals LLC

Reason
CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in specific lots of Irbesartan.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 26, 2021Historical recordClass II

Westminster Irbesartan Tablets, USP 75 mg Rx Only Manufactured by: ScieGen Pharmaceuticals, Inc. Hauppauge, NY 11788 Manufactured for: Westminster Pharmaceuticals, LLC. Olive Branch, MS 38654 a) 30 count bottle NDC 69367-119-01; b) 90 count bottle NDC 69367-119-03

by Westminster Pharmaceuticals LLC

Reason
CGMP Deviations: FDA laboratory testing confirmed traces of NDEA impurity in specific lots of Irbesartan.
Published
December 19, 2018
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 11, 2023Historical recordClass II

Thyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-1

by LGM Pharma LLC

Reason
CGMP Deviations: Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.
Published
December 19, 2018
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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