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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,266
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 181–200 of 17,412 recalls

FDA Recall Ongoing2026 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

View recall →

FDA Recall United States Ongoing2026 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

View recall →

FDA Recall United States Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 Ongoing2026 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 →

FDA Recall Ongoing2026 recordClass II

TopCare Health, CARBAMIDE PEROXIDE 6.5%, 0.5 FL OZ (15 mL) a) Kit - WASHER BULB & DROPS INCLUDED (NDC 36800-835-33); b) 1 bottle (NDC 36800-835-34), DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007.

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 Ongoing2026 recordClass II

QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (NDC 63868-026-15); b) 1 bottle (NDC 63868-027-16), Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376.

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 Ongoing2026 recordClass II

Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.

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 Ongoing2026 recordClass II

CVS Health, Carbamide Peroxide, 6.5%, 0.5 FL Oz (15 mL), a) Bottle (NDC 51316-822-00.); b) Kit (1 BULB, Syringe & Drops- NDC 51316-823-00.), Distributed by: CVS Pharmacy., Inc. One CVS Drive, Woonsocket, RI 02895,

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 Ongoing2026 recordClass II

Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35

by Padagis US LLC

Reason
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
Published
July 22, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Azacitidine for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For Subcutaneous and Intravenous Use, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0857-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

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FDA Recall Ongoing2026 recordClass II

Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01

by Reliance Life Sciences Private Limited

Reason
Lack of Sterility Assurance
Published
July 15, 2026
Distribution
Nationwide

View recall →

Data last updated:

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.