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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 October 2026.

37,212
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,841
Class I recallsReasonable probability of serious health consequences
24,366
Class II recallsTemporary or medically reversible health consequences
2,892
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 2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 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)

  • 1,714 recalls have been announced year to date.
  • Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (297).
  • Oct 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 18,381–18,400 of 23,259 recalls

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) adult gummies Multi, 150 count, UPC 0-31604-0…
Reason
Specific lots of Nature Made(R) product may have possible Salmonella contamination.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall United States Completed Historical recordClass II

Geneva Foods, LLC

Product
Lysander's All Natural Spicy Bourbon Flavor Rub; for beef, c…
Reason
Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Inland Seafood, Inc.

Product
Inland Market, Maryland Crab Cake, Net Wt. 5 lbs, Inland Mar…
Reason
Possible contamination with foreign matter; wood pieces.
Published
September 14, 2016
Distribution
CT, FL, GA, MA, MD, NC, NJ, NY, PA, SC,…

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FDA Recall United States Terminated Historical recordClass II

ConAgra Frozen Foods, Inc

Product
PF Chang's Home Menu Brand Shrimp Lo Mein, UPC 3100067005, 2…
Reason
Metal fragments were discovered in an raw ingredient used in the manufacture of frozen meal products
Published
September 14, 2016
Distribution
Product was distributed to distributors…

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made (R) Super B-Complex, KEY B VITAMINS + VITAMIN C,…
Reason
Lot No. 1173146, exp. JUL 2017 of Nature Made(R) product may have possible Staphylococcus aureus contamination. Lot No 1204001, exp. MAR 2018 of Nature Made(R) product may have possible Salmonella contamination.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) Super B-Complex, KEY B VITAMINS + VITAMIN C,…
Reason
Specific lots of Nature Made(R) product may have possible Staphylococcus aureus contamination.
Published
September 14, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Pharmavite

Product
Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3
Reason
Specific lots of Nature Made(R) Vitamin D tablets may exceed specifications for yeast/mold.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall United States Completed Historical recordClass II

Geneva Foods, LLC

Product
Lysander's Premium Teriyaki Marinade, 1 oz (28 g), polypropy…
Reason
Product contains undeclared allergens soy and wheat. Also does not declare sulfites.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)

by Clinique International

Reason
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Published
September 7, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

General Mills, Inc

Product
Case: Beyond Meat Vegetarian Indian Curry with Beyond Chicke…
Reason
General Mills today announced a voluntary recall of a limited quantity of frozen Beyond Meat Vegetarian Indian Curry with Beyond Chicken. The recall is being issued as a precaution after the producer of frozen peas used as an ingredient in this product issued a national recall for the potential presence of Listeria monocytogenes.
Published
September 7, 2016
Distribution
USA: CA, CO, CT, FL, IN, IA, MD, NH, NY…

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Blueberry Muffin Mix; NET WT 23.3 oz. (1 lb 7.3 oz) 66…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

International Foodsource, LLC

Product
IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. 30 lb.…
Reason
Raw pistachios may be contaminated with Salmonella which was determined through FDA contract laboratory testing.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Eastland Food Corporation

Product
Euro Custard Cake, Plastic wrapped cardboard container (Net…
Reason
The New York Department of Agriculture and Markets tested the Euro Custard Cake an detected that the product contained milk. The label did not declare milk and list it as an allergen on the label. Eastland Food Corporation became aware of these results on June 21 when FDA visited it facility. Eastland Food Corporation performed an investigation into the matter and determine late on June 22 that a single lot (310 cases) of product was missing this information. To this point no adverse incidents have been reported due to the mislabeling. Health risk assessment, people who have an allergy or severe sensitivity to milk run the risk of a serious or life threatening allergic reaction if they consume the affected Euro Custard Cakes under the mistaken assumption that it does not contain milk.
Published
September 7, 2016
Distribution
The cases in the lot were distributed to…

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Yellow Cake Mix; NET WT 20 z. (1 lb 4oz) 567 g); UPC…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Hampton Creek Foods

Product
JUST Chocolate Chunk Muffin Mix; NET WT 20.8 oz. (1 lb 4.8…
Reason
Firm received a positive test result for Salmonella in Coconut Milk powder which was used in the manufacturing on six cake and muffin mixes.
Published
September 7, 2016
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.