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Recall totals

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

37,205

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/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 1, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; T…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Pepper-Jack cheese. All affected product private labeled fo…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: White Colby cheese. All affected product private labeled fo…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Colby-Jack (or CoJack; Marble) cheese. All affected product…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Colby-Jack (or CoJack; Marble) cheese. All affected product…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Colby cheese. All affected product private labeled for othe…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Liquid Whey; Bulk.
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall United States Terminated Historical recordClass I

Deutsch Kase Haus, LLC

Product: Cheddar cheese. All affected product private labeled for ot…
Reason: Potential Listeria monocytogenes contamination.
Published: May 3, 2017
Distribution: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN,…

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FDA Recall Terminated Historical recordClass II

Nystatin and Triamcinolone Acetonide Cream, USP, 100,000 USP nystatin units and 1 mg triamcinolone acetonide, distributed in a) 15 grams (NDC 51672-1263-1), b) 30 grams (NDC 51672-1263-2) and c) 60 grams (NDC 51672-1263-3) tubes, Rx only, TARO label; Mfd. by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1 -- Dist. by: Taro Pharmaceuticals U.S.A. Inc., Hawthorne, NY 10532

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Failed Content Uniformity Specifications; out-of-specification (OOS) results 18-month stability
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

CLENZIderm M.D. Acne Treatment System, kit has 3 bottles a) Therapeutic Lotion (benzoyl peroxide 5% Acne Treatment) 47mL bottle, b) Daily Care Foaming Cleanser (Salicylic Acid 2% Acne Treatment) 118 mL bottle, c) Salicylic Acid 2% Acne Treatment 148mL, Valeant Pharmaceuticals North America LLC Distributed by OMP, Inc Long Beach, CA 90806 Made in USA, Product SKU 301876103018, NDC 0187-6103-01

by Valeant Pharmaceuticals North America LLC

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

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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

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

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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Data last updated: October 1, 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.