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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.

37,066
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

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 20,481 recalls

FDA Recall United States Terminated Historical recordClass II

UNFI General Corporate

Product
Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Gol…
Reason
The ingredient Triticale is not identified as wheat.
Published
February 21, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

U.S. Tov, Inc.

Product
Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code 721557…
Reason
Potential choking hazard; product contains konjac.
Published
February 21, 2024
Distribution
U.S. distribution to the following: AK,…

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FDA Recall Ongoing Historical recordClass III

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

by Amerisource Health Services LLC

Reason
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result in the repackaged product for Related Compounds (Impurities) at the 6-month time point.
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottle, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd, Oral Solid Dosage Unit, Ahmedabad 382213, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 60219-1502-01

by Amneal Pharmaceuticals of New York, LLC

Reason
Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lansoprazole Delayed-Release Capsules USP, 15 mg, 14-count bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41

by NATCO Pharma Limited

Reason
CGMP Deviations: Inadequate induction sealing on bottles, capsules were observed with bubbles on band seal, capsules with holes and spheres sticking to capsules. Also coding details were missing on one bottle.
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Medline Remedy Clinical TREAT Antifungal Cream, 2% Miconazole Nitrate, Paraben Free, 4 FL OZ (118 mL) tube, Manufactured for Medline Industries, LP Three Lakes Drive, Northfield, IL 60093. NDC: 53329-147-44

by MEDLINE INDUSTRIES, LP - Northfield

Reason
Labeling: Not Elsewhere Classified; Product labeling contains the claim of 'Paraben Free' while the product does in fact contain parabens as part of the formulation/ ingredient list.
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Febuxostat Tablets, 40 mg, 30 Tablets (3 x 10) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-538-21, NDC Unit dose 60687-538-11

by Amerisource Health Services LLC

Reason
CGMP Deviations
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-05

by Dr. Reddy's Laboratories, Inc.

Reason
Misprint on tablet
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01

by Dr. Reddy's Laboratories, Inc.

Reason
Misprint on tablet
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Up&Up brand dry eye relief (Carboxymethylcellulose 0.5%) packaged in 0.5 FL OZ (15 mL) each bottles (Twin Pack), Distributed by: Target Corporation Minneapolis, MN 55403, NDC 76168-800-30

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Rugby brand Lubricating Tears Eye Drops (Dextran 70 0.1%, Hypromellose 2910 0.3%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1282-94

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Lubricant Eye Drops (Propylene glycol 0.6%), packaged in 0.33 FL OZ (10 mL) each bottle (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-3 Retail Labeler: Rite Aid

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Multi-action Relief Drops (Polyvinyl alcohol 0.5%, Providone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-2254-3

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Lubricant Gel Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%), packaged in 0.33 FL OZ (10 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4540-3

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Lubricant Gel Drops (Carboxymethylcellulose sodium 1.0%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4540-5

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

CVS Health brand Mild Moderate Lubricating Eye Drops (Propylene glycol 400 0.25%), packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-711-15

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-5

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.34 FL OZ (10 mL) bottles, Distributed by: Walmart Inc., Bentonville, AR 72712, NDC 79903-168-01

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Velocity Pharma brand Lubricating Eye Drop (Propylene glycol Eye Drops 0.6%), packaged in 3 bottles of 0.33 FL OZ (10 mL) each, Velocity Pharma, NDC 76168-502-30

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%), packaged in 0.33 FL OZ (10 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0587-1

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
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.