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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: GU ×
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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 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 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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FDA Recall Terminated Historical recordClass II

Thiamine HCl/Pyridoxine HCl 20 mg/mL /100mg/ml Injection Solution, 30mL Amber Glass Vial, Rx only, AnazaoHealth, 7465 W. Sunset Road, Las Vegas, NV, NDC 72682-8721-3.

by AnazaoHealth Corporation

Reason: Presence of Particulate Matter.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

B-Complex, Thiamine HCI / Riboflavin / Niacinamide / Dexpanthenol / Pyridoxine HCI injection, 74/2/75/2/2 MG/ML, 30ML Sterile Multiple-Dose Vial, Rx only, AnazaoHealth, 7465 W Sunset Rd #1200, Las Vegas, NV 89113, NDC 72682-2230-3

by AnazaoHealth Corporation

Reason: Presence of Particulate Matter.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Inhub Wixela (fluticasone propionate and salmeterol inhalation powder, USP) 500/50MCG, 60 Doses of Inhalation Powder, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. NDC: 0378-9320-32

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Warfarin Sodium Tablets, USP, 5 mg, 100 Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1721-01

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Warfarin Sodium Tablets, USP, 2.5 mg, 100 Tablets per bottle, Rx only, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC: 0093-1714-01

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Triamterene and Hydrochlorothiazide Capsules, USP, 37.5 mg/25 mg, 100 capsules per bottle, Rx Only, Distributed by: Lannett Company, Inc, Philadelphia, PA 19136. NDC 0527-1632-01

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Terconazole Vaginal Suppositories, 80 mg, 3 Suppositories with Vaginal Applicator, Rx only, Manufactured by: Cosette Pharmaceuticals, Inc., 111 Coolidge Street, South Plainfield, NJ 07080. NDC: 0713-0552-73

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SPIRIVA HANDIHALER (tiotropium bromide inhalation powder) 18 mcg/Capsule, 30 capsules, 3 blister cards, each card contains 10 capsules, Rx only, For oral inhalation only, Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. NDC: 0597-0075-41

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RIVASTIGMINE TRANSDERMAL SYSTEM, Delivers 4.6 mg/24 hours, 30 systems per box, Rx Only, Distributed by: Alvogen, Inc., Morristown, NJ 07960. NDC 47781-304-03

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ricola CherryHoney Herb Throat Drops (menthol, 1.8 mg), 10 Drops per roll, Manufacturer: Ricola Ltd., 4242 Laufen, Switzerland; Distributed by: Ricola USA Inc., 6 Campus Drive, 2nd Floor South, Parsippany, NJ 07054. NDC: 54305-507-10

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Published: January 3, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Propranolol Hydrochloride Tablets, 20 mg, 100 Tablets per bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807. NDC: 69238-2078-1

by CARDINAL HEALTHCARE

Reason: CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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.