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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.

36,950
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
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 421–440 of 22,491 recalls

FDA Recall United States Ongoing 2026 recordClass II

Straus Family Creamery

Product
STRAUS FAMILY CREAMERY Cookie Dough ORGANIC SUPER PREMIUM IC…
Reason
Potential contamination with foreign objects (metal pieces).
Published
June 10, 2026
Distribution
Domestic: CA, CO, AZ, CT, FL, GA, IA, IL…

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FDA Recall United States Ongoing 2026 recordClass II

Straus Family Creamery

Product
STRAUS FAMILY CREAMERY Strawberry ORGANIC SUPER PREMIUM ICE…
Reason
Potential contamination with foreign objects (metal pieces).
Published
June 10, 2026
Distribution
Domestic: CA, CO, AZ, CT, FL, GA, IA, IL…

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FDA Recall United States Ongoing 2026 recordClass II

Straus Family Creamery

Product
STRAUS FAMILY CREAMERY Vanilla Bean ORGANIC SUPER PREMIUM IC…
Reason
Potential contamination with foreign objects (metal pieces).
Published
June 10, 2026
Distribution
Domestic: CA, CO, AZ, CT, FL, GA, IA, IL…

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FDA Recall United States Ongoing 2026 recordClass III

Sato Pharmaceutical Inc.

Product
Yunker(branded) Energy & Health Herbal Supplement with Vitam…
Reason
Product does not meet label claim for Vitamin E.
Published
June 10, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

PRED MILD, prednisolone acetate ophthalmic suspension, USP, 0.12%, 10 mL, Sterile, Rx only, Allergen, Inc., an AbbVie company, North Chicago, IL 60064, Product of France, NDC 11980-174-10.

by AbbVie Inc.

Reason
Failed Stability Specifications
Published
June 3, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass III

Nicotine Transdermal System Patch, 14 mg, 14 patches per box, Aveva, Distributed by: RUGBY LABORATORIES, Indianapolis, IN 46268, www.majorpharmaceuticals.com, NDC 0536-5895-88.

by AVEVA Drug Delivery Systems, Inc.

Reason
Failed Impurities/Degradation Specifications: Elevated levels of oxidative-related impurities, exceeding shelf-life specifications during stability testing of individual units.
Published
June 3, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Wawa Beverage Company

Product
Wawa Fruit Punch Pint (16oz), Plastic bottle
Reason
Undeclared Milk Allergen,
Published
June 3, 2026
Distribution
The product has been distributed to the…

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FDA Recall United States Ongoing 2026 recordClass I

Wawa Beverage Company

Product
Wawa Diet Lemonade Pint (16oz), Plastic bottle
Reason
Undeclared Milk Allergen,
Published
June 3, 2026
Distribution
The product has been distributed to the…

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FDA Recall United States Ongoing 2026 recordClass I

Wawa Beverage Company

Product
Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
Reason
Undeclared Milk Allergen,
Published
June 3, 2026
Distribution
The product has been distributed to the…

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FDA Recall United States Ongoing 2026 recordClass I

Wawa Beverage Company

Product
Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle
Reason
Undeclared Milk Allergen,
Published
June 3, 2026
Distribution
The product has been distributed to the…

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FDA Recall United States Ongoing 2026 recordClass II

Fly By Jing Inc.

Product
Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets.…
Reason
Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)
Published
June 3, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Legacy Bakehouse LLC

Product
giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Ba…
Reason
Products were made with recalled California Dairies milk powder due to Salmonella.
Published
June 3, 2026
Distribution
PA and WI

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FDA Recall United States Ongoing 2026 recordClass I

Legacy Bakehouse LLC

Product
Parmesan & Herb Bagel Crisps, Item Number 18139, Net Weight:…
Reason
Products were made with recalled California Dairies milk powder due to Salmonella.
Published
June 3, 2026
Distribution
PA and WI

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FDA Recall United States Ongoing 2026 recordClass I

Legacy Bakehouse LLC

Product
Butter Parsley Bagel Crisps, Item Number 18490, Net Weight:…
Reason
Products were made with recalled California Dairies milk powder due to Salmonella.
Published
June 3, 2026
Distribution
PA and WI

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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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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.