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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 28, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL), Valeant Pharmaceuticals North America LLC Distributed by OMP, Inc Long Beach, CA 90806 Made in USA. Product SKU 301876102042, NDC 0187-6102-04

by Valeant Pharmaceuticals North America LLC

Reason: Discoloration.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

The French's Food Company, LLC SUBS Reckitt Benckiser

Product: French's Crispy Jalapenos Net Wt. 5 oz. (141.7g), UPC 0 4150…
Reason: Product may contain foreign objects: rocks and metal fragments.
Published: April 26, 2017
Distribution: Product was distributed to CA, KS, MN, M…

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FDA Recall United States Terminated Historical recordClass II

Dawn Food Products Inc.

Product: SHEILA G'S EGGLESS BROWNIE BRITTLE MIX Item 02403038 50 lb…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: R&H CHOCOLATE Speedy Creme Instant Pudding and Pie Filling…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: R&H Speedy Creme Vanilla Filling Mix Item 01148908 25 pou…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mi…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: QUIK 'N CREAMY VANILLA POWDERED FILLING Item number 000141…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutiva

Product: Nutiva Nuture Vitality Organic Plant Protein Superfood 30 S…
Reason: Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Published: April 26, 2017
Distribution: Alabama, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass I

Nutiva

Product: Nutiva Nuture Vitality Organic Plant Protein Superfood 30 S…
Reason: Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Published: April 26, 2017
Distribution: Alabama, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass II

Whiskey Hill Smokehouse

Product: Kangaroo jerky, brand Trophy Series, heat treated shelf stab…
Reason: kangaroo jerky is recalled due to undeclared soy lecithin.
Published: April 26, 2017
Distribution: CA, FL, IL, MA, NC, NY, OR, OR, PA, TX,…

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FDA Recall United States Terminated Historical recordClass II

Whiskey Hill Smokehouse

Product: Elk Jerky, brand Trophy Series, heat treated shelf stable pa…
Reason: Elk jerky is recalled due to undeclared soy lecithin.
Published: April 26, 2017
Distribution: CA, FL, IL, MA, NC, NY, OR, OR, PA, TX,…

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FDA Recall United States Terminated Historical recordClass II

Whiskey Hill Smokehouse

Product: Bison Jerky, brand Trophy Series, heat treated shelf stable…
Reason: Bison jerky is recalled due to undeclared soy lecithin.
Published: April 26, 2017
Distribution: CA, FL, IL, MA, NC, NY, OR, OR, PA, TX,…

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FDA Recall United States Terminated Historical recordClass II

Whiskey Hill Smokehouse

Product: Venison Jerky, brand Trophy Series, heat treated shelf stabl…
Reason: Venison jerky is recalled due to undeclared soy lecithin.
Published: April 26, 2017
Distribution: CA, FL, IL, MA, NC, NY, OR, OR, PA, TX,…

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FDA Recall United States Terminated Historical recordClass I

Advanced Fresh Concepts Corp

Product: AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardbo…
Reason: Product may be contaminated with listeria monocytogenes
Published: April 26, 2017
Distribution: The products were packaged by AFC Franch…

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, packaged in a) 60-count bottles (NDC 59746-317-60) and b) 100-count bottles (NDC 59746-317-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, packaged in a) 60-count bottles (NDC 59746-316-60) and b) 100-count bottles (NDC 59746-316-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 100 mg, packaged in a) 60-count bottles (NDC 59746-315-60) and b) 100-count bottles (NDC 59746-315-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only, APP Fresenius Kabi USA, LLC, Lake Surich, IL 60047, NDC 63323-614-01, Distributed by McKesson Medical-Surgical, Inc.

by Mckesson Medical Surgical

Reason: Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.

by Allergan Sales, LLC

Reason: Failed Impurities/Degradation Specifications
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ESTRADIOL, USP Bulk (Hemihydrate), in a) 25 g (NDC 38779-2261-04) and b) 100 g (NDC 38779-2261-05) bottles, Packed by MEDISCA INC. PLATTSBURGH, NY Product Code 2261

by Medisca, Inc.

Reason: cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Published: April 19, 2017
Distribution: Nationwide

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Data last updated: September 28, 2026 ET

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.