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Recall totals

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

37,063

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 11, 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 Terminated Historical recordClass I

Secret, Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0

by The Procter & Gamble Company

Reason: Chemical contamination: presence of benzene
Published: January 24, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Secret, powder fresh, Aluminum chlorohydrate 24%, Anti-Perspirant/Deodorant, Topical spray can Net Wt., (a) 4OZ (113g), NDC 37000-134-11, UPC 0 37000 71109 4, (b) 6OZ (170g), NDC 37000-134-17, UPC 0 37000 71108 7; (c) twin pack-2 each can Net Wt. 6OZ (170g), NDC: 37000-134-01, UPC 0 37000 58690 6; Distr. by: Procter & Gamble, Cincinnati, OH 45202

by The Procter & Gamble Company

Reason: Chemical contamination: presence of benzene
Published: January 24, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5 mEq/mL), Glass ABBOJECT Unit of Use Syringe, For Intravenous Use, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake Forst, IL 60045, NDC 0409-5534-24 (carton), 0409-5534-14 (case).

by Pfizer Inc.

Reason: Presence of Particulate Matter; identified as glass
Published: January 24, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Freskaro refresh & revitalize Magnesium Citrate Saline Laxative Oral Solution Grape Flavor 10 fl. oz, Manufactured by: Pharma Lobis, 7400 Alumax Dr., Texarkana, TX 75501, NDC 82645-311-10.

by Pharma Nobis LLC

Reason: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published: January 24, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Good Neighbor Pharmacy, DYE FREE, SUGAR FREE Magnesium Citrate Saline Laxative, Oral Solution, Cherry Flavor 10 fl. oz, Distributed by AmerisourceBergen, 1 West First Ave, Conshochoken, PA 19428, NDC 46122-741-38

by Pharma Nobis LLC

Reason: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter nitrogenifigens bacteria.
Published: January 24, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mead Johnson & Company LLC

Product: Enfamil Nutramigen Hypoallergenic Infant Formula Powder with…
Reason: Product has the potential to be contaminated with Cronobacter sakazakii.
Published: January 24, 2024
Distribution: Nationwide

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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

Vita 360, LLC

Product: Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb…
Reason: FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.
Published: January 17, 2024
Distribution: Domestic distribution only throughout Pu…

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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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Data last updated: September 11, 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.