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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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 United States Terminated Historical recordClass II

TreeHouse Foods, Inc.

Product: Central Market 16oz Organic Low Sodium Chicken Broth Concent…
Reason: potential microbial contamination
Published: January 24, 2024
Distribution: Product Distributed to the following sta…

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FDA Recall United States Terminated Historical recordClass II

TreeHouse Foods, Inc.

Product: Full Circle, 32oz Organic Chai Tea Latte
Reason: potential microbial contamination
Published: January 24, 2024
Distribution: Product Distributed to the following sta…

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FDA Recall United States Terminated Historical recordClass II

TreeHouse Foods, Inc.

Product: Trader Joe's 32oz Turkey Stock
Reason: potential microbial contamination
Published: January 24, 2024
Distribution: Product Distributed to the following sta…

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FDA Recall United States Terminated Historical recordClass II

TreeHouse Foods, Inc.

Product: Chicken Broth sold under Chef's Cupboard, 32oz Chicken Stock…
Reason: potential microbial contamination
Published: January 24, 2024
Distribution: Product Distributed to the following sta…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product: Ministry of Snacks Sweet and Savory Collection #8700
Reason: Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed in gift baskets.
Published: January 24, 2024
Distribution: U.S. distribution to the following: AK,…

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FDA Recall Completed Historical recordClass II

Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-180-15

by Dr. Reddy's Laboratories, Inc.

Reason: Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.
Published: January 17, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, 30-count bottles, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ 08816 Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, INDIA, NDC 16571-862-03

by Rising Pharma Holding, Inc.

Reason: Presence of Foreign Tablets/Capsules
Published: January 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and b) 500 count (NDC 68180-153-02) bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202.

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the acceptable intake limit.
Published: January 17, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Vigabatrin for Oral Solution, USP 500 mg per packet, 50 packets per box, Rx Only, Manufactured by: InvaGen Pharmaceuticals, Inc., (a subsidiary of Cipla Ltd.), Hauppauge, NY, 11788, Manufactured for: Cipla USA, Inc., Warren, NJ 07059, NDC 69097-964-53

by InvaGen Pharmaceuticals, Inc.

Reason: Defective Container: powder may leak out of the pouch
Published: January 17, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tacrolimus Capsules, USP 1mg, 100-Count Bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories Limited, Bachupally, 500 090, INDIA, NDC 55111-526-01

by Dr. Reddy's Laboratories, Inc.

Reason: Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in a bottle of 1 mg Tacrolimus capsules.
Published: January 17, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Garden Spot Foods, LLC.

Product: Shiloh Farms Organic Salt Free 7 Grain Bread UPC 0-47593-021…
Reason: Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Published: January 17, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

Garden Spot Foods, LLC.

Product: Shiloh Farms Organic 7 Grain Bread UPC 0-47593-02112-8
Reason: Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Published: January 17, 2024
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

Garden Spot Foods, LLC.

Product: Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-0281…
Reason: Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
Published: January 17, 2024
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose, packaged in 6000mL bags, Rx only, Fresenius Medical Care NA Waltham, MA 02451, NDC 49230-206-62.

by Fresenius Medical Care Holdings, Inc.

Reason: Lack of Sterility Assurance
Published: January 10, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Eprontia (topiramate) oral solution, 25 mg/mL, 473 mL Bottle, Rx only, Manufactured for: Azurity Pharmaceuticals, Woburn, MA 01801, NDC 52652-9001-1

by Azurity Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification Impurity C (4,5-desisopropylidene topiramate) result observed during routine stability testing at 18 months.
Published: January 10, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

BioMylz Pvt. Ltd.

Product: Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor…
Reason: Potential mold contamination
Published: January 10, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06

by TCP HRB ACQUISITON LLC

Reason: Chemical contamination: Presence of benzene
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06

by TCP HRB ACQUISITON LLC

Reason: Chemical contamination: Presence of benzene
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA

by TCP HRB ACQUISITON LLC

Reason: Chemical contamination: Presence of benzene
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ

by Meta Herbal

Reason: Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient (API) - Sildenafil.
Published: January 3, 2024
Distribution: Nationwide

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Data last updated: September 12, 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.