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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.

37,116
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
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 7,861–7,880 of 19,382 recalls

FDA Recall Terminated Historical recordClass II

Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Dose Cups per case, NDC: 68094-204-61; Unit Dose Cup NDC: 68094-204-59], Rx only, Precision Dose, Inc., South Beloit, IL 61080

by Precision Dose Inc.

Reason
CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
Published
March 18, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC carton: 60687-322-01; NDC Unit Dose Card: 60687-322-11

by American Health Packaging

Reason
CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
Published
March 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quetiapine Fumarate Extended-Release Tablets, 300 mg, 100 tablets per unit dose carton, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454775 India; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA. NDC: 0904-6804-61

by The Harvard Drug Group

Reason
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Published
March 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Quetiapine Fumarate Extended-Release Tablets, 200 mg, 100 tablets per unit dose carton, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454775 India; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA. NDC: 0904-6803-61

by The Harvard Drug Group

Reason
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Published
March 18, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Quetiapine Fumarate Extended-Release Tablets, 150 mg, 100 tablets per unit dose carton, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454775 India; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA. NDC: 0904-6802-61

by The Harvard Drug Group

Reason
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Published
March 18, 2020
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Quetiapine Fumarate Extended-Release Tablets, 50 mg, 100 tablets per unit dose carton, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.) 454775 India; Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 USA. NDC: 0904-6801-61

by The Harvard Drug Group

Reason
Labeling; Incorrect or Missing Package Insert: Product was packaged with the package insert for Quetiapine Fumarate Tablets not Quetiapine Fumarate Extended-Release Tablets.
Published
March 18, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-858-01

by Mayne Pharma Inc

Reason
Product Mix-Up: A foreign tablet was found in bottle.
Published
March 18, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GARZA FOOD VENTURES

Product
Siete Grain Free Burrito Size Tortillas Net Wt 15 oz (423g)…
Reason
Sodium level in the product 340 mg per serving, instead of the 15 mg declared on the label.
Published
March 18, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
William R Hill brand Soup Base Chicken, Item #41178, 1 lb, m…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
MJ Kellner brand Milk Replacer, Vegan, Soy Based, Item #8028…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Shaver Foods brand Gravy Chicken, Item #35213, in 2 lb. meta…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Shaver Foods brand Gravy Beef, Item #35089, in 2 lb. metalli…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Riverside brand Brown Gravy, Item #35186, in 14 oz. metallic…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
National Food Group brand Soup Base Vegetable, Item #42526,…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Good Source brand Soup Base Beef, Item #41060, in 35 lb. pai…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Good Source brand Soup Base Chicken, Item #41535, in 35 lb.…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
American Bounty brand Icing Mix Vanilla, Item #32595, in 5 l…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
William R Hill brand Soup Base Beef, Item #41504, 1 lb, meta…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

View recall →

FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
American Bounty brand Soup Base Beef No MSG, Item #41178, 1…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

View recall →

FDA Recall United States Terminated Historical recordClass II

Tova Industries Inc

Product
Indianhead brand Vanilla Crystals, Item #80580, in 10 lb. ba…
Reason
Downstream recall from supplier. Possible metal shavings in ingredient.
Published
March 18, 2020
Distribution
Products were distributed to the followi…

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.