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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 II24,343
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 8,641–8,660 of 18,374 recalls

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Dellalo HG Pizza Flour 50lb bags Product Code 845212 Lot#…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
H&R Flour (Hotel and Restaurant) 50lb bags Product Codes 70…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Gigantic Flour 50lbs Product Code 701220 Lot #: 8346BF
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
King Arthur All Purpose Flour 5 LB bag UPC code: 071012010…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Pillsbury BEST Bread Flour Enriched 5 LB bag UPC code: 05…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Pillsbury POTENTATE HIGH GLUTEN FLOUR BLEACHED BROMATED E…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Pillsbury BALANCER HI GLUTEN FLOUR BLEACHED BROMATED ENR…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Gold Medal Flour Product Code: 805046 Bulk flour
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Miss Minneapolis Product Code: 803003 Bulk flour
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

ADM - CHICAGO

Product
Baker's Corner All Purpose Flour 5 lb. bag UPC code: 041…
Reason
potential presence of E. coli. O26
Published
July 24, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Perrigo Company PLC

Product
Parent's Choice Advantage Infant Formula Milk-Based Powder w…
Reason
Product may contain metal fragments.
Published
July 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories

by American Health Packaging

Reason
GMP Deviations: Potential cross contamination due to cleaning procedure failure.
Published
July 17, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major Pharmaceuticals 17177 N. Laurel Park Drive Suite 233, Livonia, MI 48152.

by MAJOR PHARMACEUTICALS

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
Published
July 17, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Losartan Potassium, 100 mg tablets, 90 count bottle, NDC 60429-318-90

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30

by Golden State Medical Supply Inc.

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets, USP Rx Only, Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-052-10

by Macleods Pharma Usa Inc

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-051-10

by Macleods Pharma Usa Inc

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-050-10

by Macleods Pharma Usa Inc

Reason
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Published
July 17, 2019
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.