Data Explorer

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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

State: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 8, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: January 14, 2021Historical recordClass III

Carvedilol Tablets, USP, 3.125 mg, 500-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; NDC 68382-092-05

by Zydus Pharmaceuticals USA Inc

Reason: Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid, light yellow substance, identified as a fragmented tablet of another drug product, found mixed with tablets in a bottle of Carvedilol tablets 3.125mg.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 28, 2022Historical recordClass III

Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-25

by Akorn Inc

Reason: Failed impurities/degradation specification: Out of Specification result for total impurity at 4.0% (Limit: NMT 3.0%) at 12 months stability testing.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 10, 2021Historical recordClass I

Winter Gardens Quality Foods, Inc.

Product: Chips & Chocolate, A layered dessert with chocolate mousse l…
Reason: Products potentially contaminated with Salmonella.
Published: May 1, 2019
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: April 6, 2021Historical recordClass II

Mineralife LLC

Product: Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bott…
Reason: The dietary supplement product is potentially contaminated with Pseudomonas aeruginosa
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 13, 2019Historical recordClass II

Patagonia Provisions Inc

Product: Patagonia Provisions Savory Seeds Variety Pack; Classic Bar…
Reason: Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 13, 2019Historical recordClass II

Patagonia Provisions Inc

Product: Patagonia Provisions Chipotle Lime Savory Seeds; 1 oz. poly…
Reason: Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 13, 2019Historical recordClass II

Patagonia Provisions Inc

Product: Patagonia Provisions Mellow Curry Savory Seeds; 1 oz. poly-…
Reason: Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 13, 2019Historical recordClass II

Patagonia Provisions Inc

Product: Patagonia Provisions Classic Barbecue Savory Seeds; 1 oz. p…
Reason: Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published: May 1, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 10, 2020Historical recordClass III

Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass container, Rx ONLY, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742.

by Johnson Matthey Inc.

Reason: Failed Impurities/Degradation Specifications: Unknown impurity above specification limits.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: January 19, 2022Historical recordClass I

Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah, Malaysia, UPC 9 557205 060083.

by Brian P. Richardson

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared sildenafil and tadalafil, two FDA approved drugs for the treatment of male erectile dysfunction, making this an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 8, 2020Historical recordClass II

Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in (a) 150 mL bottle (NDC 0093-4150-80) (b) 80 mL bottle (NDC 0093-4150-79), Rx Only, Manufactured in Canada By: Teva Canada Limited Toronto, Canada, M1B2K9, Manufactured For: Teva Pharmaceuticals USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason: Subpotent Product: assay results for Amoxicillin were below the specification limits.
Published: April 24, 2019
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2021Historical recordClass II