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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.

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,921–1,940 of 20,055 recalls

FDA Recall United States Terminated Historical recordClass II

Rise Baking Company, LLC dba The New French Bakery Inc.

Product
L'Oven Fresh KETO Friendly Original 6 Tortilla Wraps. Net W…
Reason
Foreign Material (metal)
Published
December 25, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Rise Baking Company, LLC dba The New French Bakery Inc.

Product
Bakestone Brothers Pita Bread, 6 Whole Wheat Pitas. Net Wt.…
Reason
Foreign Material (metal)
Published
December 25, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Rise Baking Company, LLC dba The New French Bakery Inc.

Product
Bakestone Brothers Pita Bread, 6 White Pita. Net Wt. 11.4 o…
Reason
Foreign Material (metal)
Published
December 25, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Stuyvers Bread (Premium Brand Bakery Division)

Product
Baguette, Artisan Multigrain. (30 Units/box) 400g/each. Cont…
Reason
Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product
Published
December 25, 2024
Distribution
product was distributed to two consignee…

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FDA Recall United States Terminated Historical recordClass II

Stuyvers Bread (Premium Brand Bakery Division)

Product
Pull apart Holiday Rolls (cluster bun). (2 Units/bag) 195g/e…
Reason
Possible contamination by a foreign object (metal) in sub-ingredient in dinner roll product
Published
December 25, 2024
Distribution
product was distributed to two consignee…

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FDA Recall United States Terminated Historical recordClass II

Impossible Foods Inc

Product
Impossible Spicy Ground Sausage Meat from plants 14oz chub,…
Reason
product may contain pieces of metal
Published
December 25, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Impossible Foods Inc

Product
Impossible Savory Ground Sausage Meat from plants 14oz chub,…
Reason
product may contain pieces of metal
Published
December 25, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-040-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 150 mcg (0.150 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-445-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 137 mcg (0.137 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-041-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-443-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 42292-039-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 100 Tablets per carton (10 unit dose blister cards of 10 tablets each), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC: 51079-442-20

by Mylan Institutional, Inc.

Reason
Subpotent and Superpotent Drug
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dabigatran Etexilate, 150mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-475-60

by Ascend Laboratories, LLC

Reason
CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dabigatran Etexilate, 75 mg capsules, 60-count bottles, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-474-60

by Ascend Laboratories, LLC

Reason
CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets USP, 112 mcg, packaged in a) 90-count bottles (NDC 0378-1811-77) and b) 1000-count bottles (NDC 0378-1811-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

by Viatris Inc

Reason
Superpotent Drug and Subpotent Drug: potency failures obtained
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC 0378-1809-77) and b) 1000-count bottles (NDC 0378-1809-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

by Viatris Inc

Reason
Superpotent Drug and Subpotent Drug: potency failures obtained
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets USP, 88 mcg, packaged in a) 90-count bottles (NDC 0378-1807-77) and b) 1000-count bottles (NDC 0378-1807-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

by Viatris Inc

Reason
Superpotent Drug and Subpotent Drug: potency failures obtained
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets USP, 75 mcg, packaged in a) 90-count bottles (NDC 0378-1805-77) and b) 1000-count bottles (NDC 0378-1805-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

by Viatris Inc

Reason
Superpotent Drug and Subpotent Drug: potency failures obtained
Published
December 18, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Levothyroxine Sodium Tablets USP, 50 mcg, packaged in a) 90-count bottles (NDC 0378-1803-77) and b) 1000-count bottles (NDC 0378-1803-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.

by Viatris Inc

Reason
Superpotent Drug and Subpotent Drug: potency failures obtained
Published
December 18, 2024
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.