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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 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

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)

  • 1,527 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

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

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,761–2,780 of 18,346 recalls

FDA Recall Terminated Historical recordClass III

MYDRIATIC-4: Tropicamide - Proparacaine - Phenylephrine - Ketorolac Sterile Ophthalmic Solution Drops 1% - 0.5% - 2.5% - 0.5%, 5mL bottle, Imprimis, NJOF, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852 (844)-446-6979, NDC:71384-632-05

by Imprimis NJOF, LLC

Reason
Subpotent: Out of Specification result observed for Ketorolac assay levels, below the 90.0-110.0% of label claim.
Published
October 25, 2023
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

HEINZ

Product
Kraft Singles American Pasteurized Prepared Cheese product,…
Reason
Plastic fragment. Product is recalled due to potential for a thin strip of the primary packaging film to remain adhered to the cheese slice after the wrapper has been removed.
Published
October 25, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass I

BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04

by Scynexis, Inc.

Reason
Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).
Published
October 18, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Little Oak Company Ltd

Product
LittleOak Natural Goat Milk Follow On Infant Formula (Stage…
Reason
No pre-market notification and Mixing instructions not in ounces
Published
October 18, 2023
Distribution
WY, CA, NY, GA, IL, UT, MD, CO, PA, VT,…

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FDA Recall United States Terminated Historical recordClass II

The Little Oak Company Ltd

Product
LittleOak Natural Goat Milk Infant Formula (Stage 1); packag…
Reason
No pre-market notification and Mixing instructions not in ounces
Published
October 18, 2023
Distribution
WY, CA, NY, GA, IL, UT, MD, CO, PA, VT,…

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FDA Recall Ongoing Historical recordClass II

Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40mg/mL), 10 mL Multiple Dose Vial, Rx Only, For Intramuscular or Intra-articular use only, Shake Well, Not for IV/ID, intraocular, epidural, or intrathecal use, Mfd. in India for Auromedics Pharma LLC., E Windsor, NJ, 08520, NDC 55150-385-01.

by Eugia US LLC

Reason
Presence of Particulate Matter: A product complaint of a piece of glass was identified in a vial. The piece of glass appears to be roughly 1 cm x 0.5 cm inside the vial.
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01 Not for resale. Office use only. Lot: 23APR018 Date Compounded: 24APR2023 Expires on: 17APR2024. In case of adverse event contact: www.fda.gov/medwatch or (800)-FDA-1088 Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852 (844) 446-6979

by Imprimis NJOF, LLC

Reason
Subpotent: Failing Test Results for Epinephrine
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11

by Amerisource Health Services LLC

Reason
Failed Impurities/Degradation Specifications: Out of Specification results in the repackaged product for impurities at the 12-month time point.
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxybutynin Chloride Extended-Release Tablets USP 10 mg, a) 100 tablets (NDC 68382-256-01) and b) 500 tablets (NDC 68382-256-05) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Dissolution Specifications
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, UPC 00854582001111.

by Dr. Berne's Whole Health Products

Reason
Non-Sterility
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, UPC 00854582001111.

by Dr. Berne's Whole Health Products

Reason
CGMP Deviations
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dr. Berne's Organic Castor Oil Eye Drops, Net WT 30 mL/1 fl oz bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, Certified Organic by Organic Certifiers.

by Dr. Berne's Whole Health Products

Reason
CGMP Deviations
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dr. Berne's MSM MIST 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com.

by Dr. Berne's Whole Health Products

Reason
CGMP Deviations
Published
October 11, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Dr. Berne's MSM DROPS 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, hello@drsamberne.com, UPC 00854582001036

by Dr. Berne's Whole Health Products

Reason
CGMP Deviations
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in dextrose 5%, 0.5 mg/5 mL, (0.1 mg/mL), 5 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2012-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in 0.9% Sodium Chloride, 30 mg/30 mL, (1 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2012-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in dextrose 5%, 3 mg/30 mL, (0.1 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2013-2

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in 0.9% sodium chloride, 15 mg/30 mL, (0.5 mg/mL), 30 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2011-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in 0.9% sodium chloride, 10 mg/50 mL, (0.2 mg/mL), 50 mL Syringe, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC 71286-2010-2

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone in 0.9% sodium chloride, 6 mg/30 mL, (0.2 mg/mL), 30 mL Syringe, Rx only, CAPS, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2010-1

by Central Admixture Pharmacy Services Inc

Reason
Lack of assurance of sterility:
Published
October 11, 2023
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.