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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 4,661–4,680 of 20,260 recalls

FDA Recall Terminated Historical recordClass III

Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, [100 or 1000 ] Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC 100 Count bottle: 0527-1632-01; NDC 1,000 bottle: 0527-1632-10

by Lannett Company Inc.

Reason
Failed Impurity/Degradation Specifications
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Triamterene and Hydrochlorothiazide Capsules, USP (37.5 mg/25 mg), Rx Only, 1000 Capsules per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 0527-1632-10

by Lannett Company Inc.

Reason
Failed Impurity/Degradation Specifications
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tobramycin Ophthalmic Solution, USP, 0.3%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045; Distributed by: MWI, Boise, ID 83705. NDC 13985-604-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Tobramycin Ophthalmic Solution, USP, 0.3%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-290-10

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution, USP, 0.5%, Packaged in (a) 5 mL dropper bottle, NDC 17478-288-10; (b) 10 mL dropper bottles: NDC 17478-288-11; (c) 15 mL dropper bottles, NDC 17478-288-12; Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045.

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Sodium Chloride Ophthalmic Ointment, USP, 5%, Net Wt. 3.5 g (1/8 oz.) per tube, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-622-35

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL per bottle, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Distributed By: MWI Boise, ID 83705, NDC: 13985-611-15

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5%, 15 mL per dropper bottle, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031 NDC: 17478-263-12

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

PAREMYD (hydroxyamphetamine hydrobromide/ tropicamide ophthalmic solution) 1%/0.25%, 15 mL per dropper bottle, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-704-12

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 60429-957-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL (0.17 FL OZ) per bottle, Antihistamine and Redness Reliever, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC: 51407-499-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Olopatadine HCl Ophthalmic Solution, USP 0.2%, 2.5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-305-12

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Olopatadine HCL Ophthalmic Solution, USP 0.1%, Antihistamine and Redness Reliever, 5 mL (0.17 FL OZ) per bottle, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-308-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Olopatadine HCl Ophthalmic Solution, USP 0.1%, 5 mL per dropper bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-105-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Ofloxacin Ophthalmic Solution, USP 0.3%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045; Distributed by: MWI, Boise, ID 83705. NDC: 13985-602-05

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Neomycin and Polymyxin B Sulfates, and Bacitracin Zinc Ophthalmic Ointment, USP, Net Wt. 3.5 g (1/8 oz.), Rx Only, Manufactured by: Akorn, INC., Lake Forest, IL 60045. NDC: 17478-235-35

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Moxifloxacin Ophthalmic Solution, USP, 0.5%, 3 mL per dropper bottle, Rx only, Manufactured by: Akorn, Lake Forest, IL 60045. NDC: 17478-519-19

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Lidocaine Hydrochloride Jelly USP, 2%, Packaged as (a) 5 mL tube (NDC 17478-711-10) x10 per box NDC 17478-711-31; (b) 30 mL tube NDC 17478-711-30; Rx only, Manufactured by: Akorn, Inc., Lake Forest, Il 60045.

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Levofloxacin Ophthalmic Solution 0.5%, 5 mL per bottle, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, Il 60045. NDC: 17478-106-10

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Ketorolac Tromethamine Ophthalmic Solution, 0.5%, Packaged as a) 10 mL dropper bottle, NDC 17478-209-11; (b) 3 mL dropper bottle, NDC 17478-209-19; (c) 5 mL dropper bottle, NDC 17478-209-10; Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045.

by Akorn, Inc.

Reason
CGMP Deviations:
Published
January 25, 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.