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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 1,941–1,960 of 21,559 recalls

FDA Recall Ongoing Historical recordClass II

Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6 72008 80925 3

by Brands International Corporation

Reason
CGMP Deviations: lack of adequate release testing.
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Braga Fresh Foods LLC

Product
Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2…
Reason
Potential contamination with Listeria monocytogenes.
Published
January 29, 2025
Distribution
Walmart retail stores: AK, AR, AZ, CA, C…

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FDA Recall Terminated Historical recordClass II

Cardura XL (doxazosin) extended release tablets 4 mg, 30 -count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-078-93

by Viatris Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV 26505, NDC 58151-079-93

by Viatris Inc

Reason
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

glipiZIDE, Extended-Release Tablets, 2.5 mg, 30-count (3x10 blister cards) carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC: 60687-480-21, Unit Dose NDC: 60687-480-11

by Amerisource Health Services LLC

Reason
Failed Dissolution Specifications:
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Clobazam Tablets, 10 mg, packaged in 30 tablets per carton (3x10 blister cards each), Rx Only, Amneal Pharmaceuticals LLC, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 60687-423-11

by Amerisource Health Services LLC

Reason
Presence of Foreign Tablets/Capsules
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Systane Lubricant Eye Drops, Ultra PF, Sterile, 25 Vials (0.7mL Each), Manufactured for: Alcon Laboratories, Inc. Forth Worth, TX 76134

by Alcon Research LLC

Reason
Non-Sterility
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46, Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8026-02.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E., Suite 117, Fairfield, NJ 07004, NDC 71399-8028-2.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8028-1.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.

by Akron Pharma, Inc.

Reason
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Abbey Specialty Foods

Product
Wicklow Gold Cheddar Tomato & Herb, 5.2 oz., plastic cryo-va…
Reason
Product may have Listeria Monocytogenes.
Published
January 22, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Terminated Historical recordClass I

Abbey Specialty Foods

Product
Wicklow Gold Cheddar Nettle & Chive Cheese, 5.2 oz., plastic…
Reason
Product may have Listeria Monocytogenes.
Published
January 22, 2025
Distribution
The recalled product was distributed to…

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FDA Recall United States Terminated Historical recordClass III

Eclectic Institute Inc

Product
Eclectic Herb Vitamin Herb Blend vita biotic dietary supplem…
Reason
Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger Fruit and their quantities were not listed correctly in the Supplement Facts panel.
Published
January 22, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Summit Import Corporation

Product
Yu Yee, Five Spice Powder,1.76oz
Reason
Product tested and found high levels of lead.
Published
January 22, 2025
Distribution
The product was distributed to the follo…

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules USP 20 mg, 60 count bottles, Rx only, Distributed by: Rising Pharm Holdings, Inc., East Brunswick, NJ NDC 57237-017-60

by Rising Pharma Holding, Inc.

Reason
CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
Published
January 15, 2025
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 1000-count bottles, Rx Only, Manufactured by: Granules India Limited, Hyderabad- 500 081, India, Manufactured for: Quallent Pharmaceuticals Health LLC, Grand Cayman, Grand Cayman Islands, NDC 82009-117-10

by Granules Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets/Capsules: A Paracetamol 500 mg tablet was found in a 1000-count bottle of Metformin HCL ER Tablets USP, 500 mg.
Published
January 15, 2025
Distribution
Distributor in OH.

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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.