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Recall totals

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

37,060

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 9, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass III

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 30 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-034-01

by Granules Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 20 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-032-01

by Granules Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-031-01

by Granules Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 10 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-030-01

by Granules Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 5 mg, 100 Capsules, Rx only, Manufactured by: Granules Pharmaceuticals Inc., Chantilly, VA 20151, NDC 70010-029-01

by Granules Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications:
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

edunn clarity, BP Treatment Cleanser 10% (Benzoyl Peroxide 10%), 7 oz (201g) Uptown Medi Spa, Phoenix, AZ.

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

Micronized BPO Gel Cleanser 10% (Benzoyl Peroxide 10%) Pantea MD , 7 oz (201 g), University Skin Institute, 650 University Ave, Ste 200, Sacramento, CA 95825.

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

mel rx Skin, NO DRAMA Benzoyl Peroxide 10% Acne Treatment, 7 oz, 201 g Mel Skin Rx Beverly Hills, CA 90210

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

Torrey Pines Dermatology & Laser Center Benzaderm BPO Cleanser 10% (Benzoyl Peroxide 10%) 7oz (201 g), Torreypines.com

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

Skin MD by Dr Monika Kiripolsky, Body Acne Cleanser (Benzoyl Peroxide 10%), 7 oz (201 g), Monika Kiripolsky, MD Beverly Hills, CA, 90211

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

ARTISAN OF SKIN (Benzoyl Peroxide 10%) , 7 oz (201 g), Artisan of Skin Beverly Hills, CA 90210

by Private Label Skin Care Inc.

Reason: Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Published: October 1, 2025
Distribution: CA, GA only

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FDA Recall Ongoing Historical recordClass II

Azelaic Acid Gel, 15%, 50 grams, For Topical Use Only, Rx only, Manufactured by: Glenmark Pharmaceuticals Limited Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-626-52

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations: Market complaints received for gritty texture (grainy)
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

TopCare Health 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 36800-589-14

by Consumer Product Partners, LLC

Reason: Cross Contamination with Other Products.
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Kroger 70% Isopropyl Alcohol, NET WT 5.5 OZ (156 g) per can, Distributed By The KROGER CO., Cincinnati, Ohio 45202. NDC: 30142-810-14

by Consumer Product Partners, LLC

Reason: Cross Contamination with Other Products.
Published: October 1, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Domino Foods Inc

Product: PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distribu…
Reason: Potential contamination with foreign objects.
Published: October 1, 2025
Distribution: CA and UT

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FDA Recall United States Terminated Historical recordClass III

SUNGAL INC

Product: UDK ,Half Plum, 170 g, Container, 24, ambient
Reason: Cyclamate adulteration
Published: October 1, 2025
Distribution: The adulterated product was distributed…

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FDA Recall United States Completed Historical recordClass I

Gooder Foods, Inc.

Product: GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR A…
Reason: Undeclared allergens (cashews).
Published: October 1, 2025
Distribution: Foreign Distribution: Canada U.S. Distr…

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FDA Recall United States Completed Historical recordClass I

Gooder Foods, Inc.

Product: GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SP…
Reason: Undeclared allergens (milk).
Published: October 1, 2025
Distribution: Foreign Distribution: Canada U.S. Distr…

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FDA Recall Ongoing Historical recordClass II

Kit for the Preparation of Technetium Tc 99m Mertiatide, Rx Only, Manufactured by: Sun Pharmaceutical Industries, Inc. Billerica, MA 01821, NDC 45567-0655-1

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Published: September 24, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Entecavir Tablets, USP, 1 mg, 30 Tablets, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-921-06.

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Impurity/Degradation Specifications
Published: September 24, 2025
Distribution: Nationwide

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Data last updated: September 9, 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.