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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
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 2,085 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 1,961–1,980 of 19,874 recalls

FDA Recall OngoingHistorical recordClass I

FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7

by SHOPPERS- PLAZA

Reason
Marketed without an Approved NDA/ANDA; FDA laboratory analysis confirmed product tainted with undeclared metformin and glyburide
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

First Aid Beauty Ultra Repair Cream, colloidal oatmeal 0.5%, Coconut Vanilla, Net Wt. 396.8 g (14 OZ), DISTR. BY: First Aid Beauty LTD, Newton, MA, 02458, UPC 8 15517 02955 6

by First Aid Beauty Ltd

Reason
CGMP Deviations; product intended for quarantine was inadvertently distributed
Published
January 29, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical 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 OngoingHistorical 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 TerminatedTerminated: November 12, 2025Historical 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 TerminatedTerminated: November 12, 2025Historical 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 TerminatedTerminated: April 16, 2026Historical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 TerminatedTerminated: January 15, 2025Historical 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 TerminatedTerminated: March 25, 2025Historical recordClass I

The Kroger Co

Product
BOAR'S HEAD HUMMUS VEG PLATTER MED, 5 lb., packaged in a pla…
Reason
Platters and trays prepared in-store may contain cut cucumbers that were previously recalled due to potential contamination with Salmonella.
Published
January 22, 2025
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: March 25, 2025Historical recordClass I

The Kroger Co

Product
BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a pl…
Reason
Platters and trays prepared in-store may contain cut cucumbers that were previously recalled due to potential contamination with Salmonella.
Published
January 22, 2025
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: March 25, 2025Historical recordClass I

The Kroger Co

Product
SMALL VEGGIE PLATTER, 32 oz., packaged in a plastic containe…
Reason
Platters and trays prepared in-store may contain cut cucumbers that were previously recalled due to potential contamination with Salmonella.
Published
January 22, 2025
Distribution
Multiple states

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.

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