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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.

37,268
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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 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 1,141–1,160 of 21,683 recalls

FDA Recall OngoingHistorical recordClass II

Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL (34 fl. oz.) per bag (NDC 61924-092-34), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Bromocriptine Mesylate Capsules, USP, 5 mg, 30 Capsules per bottle, Rx Only. Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals, Pennington, NJ 08534. NDC 68382-110-06

by Zydus Pharmaceuticals (USA) Inc

Reason
Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90

by Golden State Medical Supply Inc.

Reason
Failed Dissolution Specifications
Published
November 26, 2025
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass III

Klarity-C Drops (Cyclosporine) 0.1%, Preservative-Free Sterile Ophthalmic Emulsion, This is a compounded drug, Office Use Only, 5.5 mL bottle, Rx only, Mfg by: Imprimis NJOF, LLC, 1705 Route 46 West, Ledgewood, NJ 07852, NDC 71384-514-05

by Imprimis NJOF, LLC

Reason
Subpotent Drug
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass III

Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-175-30

by Alembic Pharmaceuticals Limited

Reason
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: July 31, 2026Historical recordClass I

BULK & ORGANIC LLC

Product
Bulk and Organic Organic Moringa Powder, 44.1lbs bag
Reason
Possible Salmonella Richmond
Published
November 26, 2025
Distribution
Multiple states

View recall →

FDA Recall United States OngoingHistorical recordClass I

New Hoque and Sons, Inc.

Product
Dry Ghoinnya Fish
Reason
Un-eviscerated fish may be contaminated with Clostridia botulinum.
Published
November 26, 2025
Distribution
NY and NJ

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom White Elephant powder is packaged in…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom Red Bali powder is packaged in seal m…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: March 26, 2026Historical recordClass I

Lotus Vaping Technologies, LLC

Product
Monarch Premium Kratom Green Maeng Da powder is packaged in…
Reason
Product has the potential to be contaminated with Salmonella
Published
November 19, 2025
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.