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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.

36,949
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
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 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/foods-alive-recalls-organic-moringa-leaf-powder-because-possible-health-riskPublished September 4, 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)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% 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 II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 361–380 of 17,945 recalls

FDA Recall Ongoing 2026 recordClass I

MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pharmacal 1 Pharmacal Way, P.O. Box 198, Jackson, WI 53037.

by Wisconsin Pharmacal Company

Reason
Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

fentaNYL Citrate, Sterile CADD for Injection, 2,2500 mcg/50mL in Sterile Water, IntegraDose Compounding Services LLC, 3650 Victorie St N, Suite 900, Shoreview, MN, NDC 71139-6030-1.

by IntegraDose Compounding Services LLC

Reason
Subpotent Drug
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

cimzia (certolizumab pegol), 2x200mg/mL PREFILLED SYRINGES (2 single-dose), Rx ONLY, Manufactured by: UCB Inc., Smyrna, GA 30080, a) NDC 50474-710-79, b) Professional sample, NDC 50474-710-80; c) 3 cartons, STARTER KIT, NDC 50474-710-81.

by UCB Biosciences Inc.

Reason
Lack of Assurance of Sterility
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Erythromycin Tablets, USP, 500 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; (NDC 70710-1048-3).

by Zydus Pharmaceuticals (USA) Inc

Reason
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Erythromycin Tablets, USP, 250 mg, 30 tablets per bottle, Rx only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; a) 30 count bottles (NDC 70710-1047-3); b) 100 count bottles (NDC 70710-1047-1).

by Zydus Pharmaceuticals (USA) Inc

Reason
CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Estradiol Gel, 0.1%, 0.25 mg, 0.25 g per packet, 30 packets per carton, Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623. NDC 70954-531-20

by ANI Pharmaceuticals, Inc.

Reason
Defective Container; packets were found to be either empty or partially full.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Gas-X, Simethicone 125 mg/ ANTIGAS, 120 SoftGels, Distributed by: Haleon, Warren, NJ 07059, UPC: 3 00674 35041 9.

by Haleon US Holdings LLC

Reason
Labeling: Not Elsewhere Classified- Incomplete inactive ingredient information on the carton labeling.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur 441108, INDIA, a) 2 Pens- NDC 70748-346-02; b) 3 Pens - NDC 70748-346-03.

by Lupin Pharmaceuticals Inc.

Reason
Presence of particulate matter: a white thread-like structure in the cartridge
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Busulfan Injection, 60 mg per 10 mL (6 mg per mL), 8x10 mL Single-Dose Vials, Rx only, Mfd. for Sagent Pharmaceuticals, Schaumburg, IL 60195, Made in Canada, NDC 25021-241-10.

by Sagent Pharmaceuticals

Reason
Failed Impurities/Degradation Specifications
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Primidone Tablets, USP, 50 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-202-01; Individual Dose NDC: 68084-202-11

by Amerisource Health Services LLC

Reason
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Primidone Tablets, USP, 250 mg, 100 Tablets (10 x 10 unit dose blister) per carton, Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC: 68084-203-01; Individual Dose NDC: 68084-203-11

by Amerisource Health Services LLC

Reason
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Primidone Tablets, USP, 250 mg, 100-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-638-01

by Golden State Medical Supply Inc.

Reason
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Primidone Tablets, USP, 50 mg, 50-count bottle, RX only, Manufactured by: Lannett Company, Inc., Marketed by: GSMS, Incorporated, Camarillo, CA 93012. NDC 51407-637-05

by Golden State Medical Supply Inc.

Reason
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1231-01.

by Lannett Company Inc.

Reason
Cross contamination with other products: API contaminated with trace amounts of Acemetacin API.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

JOHN B SANFILIPPO & SONS INC

Product
Squirrel Brand Travelers Mix 16 oz can UPC 07223899166, 12 c…
Reason
potential presence of Salmonella
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
Non Fat Dry Milk 1#, Part #: 02000014P. Net Wt 1 lb (453g)…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
1P Jalapeno Heat Unit for 300 lbs of Meat, Part #: 18000294…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

PS Seasoning & Spices, Inc.

Product
1P Original Smokehouse Unit for 300 lbs. of Meat, Part #: 18…
Reason
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Terminated 2026 recordClass II

Wellnov Supplements LLC

Product
FulviLife Complex. Dosage:2 tablespoons (30mL). Liquid. Pack…
Reason
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Published
May 27, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

JOHN B SANFILIPPO & SONS INC

Product
Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941,…
Reason
potential presence of Salmonella
Published
May 27, 2026
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.