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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.

37,115
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 7,041–7,060 of 17,327 recalls

FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
BROCCOLI FLORETS CV BROCCOLI STEAMED and served on the sala…
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
TOFU SALAD SWEET CHILE served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
PIZZA PESTO GREEN VEGGIE served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
SLAW COCONUT CITRUS served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
BROCCOLI ROASTED PALEO served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
BROCCOLI ROASTED BUFFALO served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Caulilini, Roasted Grape & Curry Vinaigrette Cindy's served…
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Salad Bar, Trend Alert Pickled Pear & Brussels Sprouts serv…
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Salad Bar, Brussels Sprouts Shredded served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

WHOLE FOODS MARKET

Product
Caulilini, Roasted with Roasted Garlic served on the salad b…
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Caulilini & Broccoli Lemon Caper served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

WHOLE FOODS MARKET

Product
Wedge Greek Salad served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

WHOLE FOODS MARKET

Product
Vegetable Power Blend served on the salad bar
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

WHOLE FOODS MARKET

Product
Trend Alert Caulilini with Vadouvan Curry served on the sala…
Reason
Possible contamination with Listeria monocytogenes
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Gold Standard Baking, Inc.

Product
Freshness Guaranteed Croissants in clear plastic 12oz clamsh…
Reason
Product is missing ingredient and nutrition label on bottom of clamshell retail package. Missing ingredients include allergens MILK, WHEAT, and SOY
Published
December 25, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Mirtazapine Tablets, USP, 7.5 mg, 500-count tablets, Rx only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810 NDC 13107-001-05

by AuroMedics Pharma LLC

Reason
Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg tablets, 500-count bottles, contain 500-count bottles of Mirtazapine 15mg tablets labelled as Mirtazapine 7.5 mg tablets.
Published
December 18, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Mirtazapine Tablets, USP, 15 mg, 500-count tablets, Rx only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810 NDC 13107-031-05

by AuroMedics Pharma LLC

Reason
Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg tablets, 500-count bottles, contain 500-count bottles of Mirtazapine 15mg tablets labelled as Mirtazapine 7.5 mg tablets.
Published
December 18, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Petroleum jelly (White Petrolatum) USP 100%, packaged in a) 1 oz tube (UPC 1182298884), b) 2.5 oz tube (UPC 1182298541), Distributed by Rite Aid, 30 Hunter Lane, Camp Hill, PA 17011

by OraLabs, Incorporated

Reason
Cross contamination with other products: undeclared contaminants of phenol and camphor in petroleum jelly tubes.
Published
December 18, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine HCl 2% 5 mL, Syringe, Rx Only, SCA Pharmaceuticals 755 Rainbow Road Windsor, CT 08695 NDC 70004-0723-09

by SCA Pharmaceuticals, LLC

Reason
Presence of Foreign Substance: Foreign material found inside the vial (manufacturer).
Published
December 18, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited Plot No. B-25, MIDC, Shendra Aurangabad, Maharashtra -431210, India Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430

by Glenmark Pharmaceuticals Inc., USA

Reason
Defective delivery system; product is not foaming or is coming out as liquid.
Published
December 18, 2019
Distribution
Nationwide

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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.