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Recall totals

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

36,949

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,732

Class I recallsReasonable probability of serious health consequences

24,263

Class II recallsTemporary or medically reversible health consequences

2,873

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 2,071 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 5, 2026 ET

Summary (Year to date)

1,458 recalls have been announced year to date.
Aug 2026 was 53% 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	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,263
Class I	9,732
Class III	2,873
Not Yet Classified	1

FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Bag: 55154-3559-0; NDC Blister: 0904-6950-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Carton: 55154-3558-0; NDC Blister: 0904-6949-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6956-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6955-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 112 mcg (0.0112 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6954-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6952-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6951-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6950-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. NDC: 0904-6949-61

by MAJOR PHARMACEUTICALS

Reason: Subpotent Drug
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Total Nutrition Inc

Product: 1. TNVitamins 100% Organic Moringa Capsules 1,200 mg 2.…
Reason: Contaminated with Salmonella
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Modern Warrior Life, LLC

Product: Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
Reason: FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
Published: July 29, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31

by CareFusion 213, LLC

Reason: Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-10.

by Chiesi USA, Inc.

Reason: Lack of Assurance of Sterility
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

meijer, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Washer Bulb included, NDC 41250-835-33, DIST. BY MEIJER DISTRIBUTION, INC., GRAND RAPIDS, MI 49544.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL OZ DROPS, (NDC 70000-0689-1); b) 1 bottle (NDC 70000-0688-1), DIST. BY CARDINAL HEALTH, DUBLIN, OH 43017.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

GOOD NEIGHBOR PHARMACY, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit - Washer Bulb Included, (NDC 46122-556-05); b) 1 bottle (NDC 46122-557-05), Distributed by: AmerisourceBergen, 1 West First Avenue, Conshohocken, PA 19428.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included, (NDC 55319-835-01), DISTRIBUTED BY: MIDWOOD BRANDS LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

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FDA Recall Ongoing 2026 recordClass II

AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.

by Bell Pharmaceuticals, Inc

Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
Published: July 22, 2026
Distribution: Nationwide

View recall →

Data last updated: September 5, 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.