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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.

37,239
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,844
Class I recallsReasonable probability of serious health consequences
24,383
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 2,084 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eden-brothers-recalls-calabrese-broccoli-seeds-due-possible-salmonella-contaminationPublished October 7, 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)

  • 1,739 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 II24,383
Class I9,844
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,383
Class I9,844
Class III2,897
Not Yet Classified2

Showing 17,801–17,820 of 21,658 recalls

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Hydroxocobalamin 5000IU/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Hydroxocobalamin 1mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Glutathione 300 mg/1.5 mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Glutathione 200 mg/mL SVN Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Gent 80 mg/Liter Nasal, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Furosemide 20 mg/mL svn Sol, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Folic Acid Injection 5 mg/mL,10 mg/mL, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Depo-Testadiol 10/5mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Dep-Estradiol 10 mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Cyclosporine 1% Opth Sol, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Butor/Nal/Hydro Nasal Susp, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Boric Acid 1% Ear Drop, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Bladder Mixture Prep, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

B-12 1000/B6 1000 mcg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

AMP50/B121MG Complex Mix/ML Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Ace-Promazine 10 mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: October 1, 2016Historical recordClass II

Prostin Injection 10 mcg/mL, 25 mcg/mL, 50 mcg/mL, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938

by Western Drug

Reason
Lack of Assurance of Sterility
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 11, 2018Historical recordClass II

Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250 g) (NDC 54162-335-02), b) Net wt. 16.9 oz (500 g) (NDC 54162-335-05), Distributed by: Geritrex Corporation, Mount Vernon, NY 10550

by Geritrex Corp

Reason
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 11, 2018Historical recordClass II

GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories, 12-count box, Rx only, Distributed by Geritrex Corporation Mount Vernon, NY 10550, NDC 54162-015-12

by Geritrex Corp

Reason
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Published
December 9, 2015
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 11, 2018Historical recordClass II

Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube, .5 oz (15 g), Rx Only For topical use only, Distributed byGeritrex Corporation 144, Mount Vernon, NY 10550, NDC 54162-016-15

by Geritrex Corp

Reason
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
Published
December 9, 2015
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.