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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 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 781–800 of 22,519 recalls

FDA Recall Ongoing 2026 recordClass III

Eptifibatide Injection, 75 mg/100 mL vial for weight-adjusted bolus dosing, 1x100 mL Single-dose Vial, For Intravenous Use Only, Rx Only, Manufactured by: Hainan Poly Pharm. Co., Ltd., Guilinyang Economic Development Area, Haikou, Hainan Province, China 571127; Distributed by: Slate Run Pharmaceuticals, LLC, Columbus, Ohio 43215. NDC Slate Run Carton Label: 70436-027-80; NDC ProRx Carton Label: 70436-163-80

by Slate Run Pharmaceuticals

Reason
Labeling: Not Elsewhere Classified. The carton for Eptifibatide Injection 75 mg/100 mL states 75 mg/100 mL vial for weight-adjusted bolus dosing. The approved statement is 75 mg/100 mL vial for weight-adjusted infusion.
Published
March 4, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.

by AvKARE

Reason
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
Published
March 4, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, Manufactured by: LEO Pharma A/S. Industriparken 55, DK-2750 Ballerup, Denmark, Distributed by: LEO Pharma Inc., Madison, NJ 07940, USA,

by LEO PHARMA INC

Reason
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
Published
March 4, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass I

Navitas, LLC.

Product
NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) IN…
Reason
Potential contamination with Salmonella.
Published
March 4, 2026
Distribution
U.S. Distribution: CA, CO, CT, FL, GA, I…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product
Fish Ball, Frozen, 4 pieces per pack, 5lbs Wt. UPC# 81009389…
Reason
Undeclared allergen ingredient (Wheat and Sesame)
Published
March 4, 2026
Distribution
Product was distributed to 50 consignees…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product
Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 8100938…
Reason
Undeclared allergen ingredient (Wheat and Sesame)
Published
March 4, 2026
Distribution
Product was distributed to 50 consignees…

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FDA Recall United States Terminated 2026 recordClass I

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING

Product
Fish Ball, Frozen, 40 pieces per pack, 200g Wt. UPC# 8100938…
Reason
Undeclared allergen ingredient (Wheat and Sesame)
Published
March 4, 2026
Distribution
Product was distributed to 50 consignees…

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FDA Recall United States Ongoing 2026 recordClass I

Prime Food Processing LLC.

Product
Prime Food Processing Dried Croaker Fish; NET WT: 8oz (227g)…
Reason
Uneviscerated Fish
Published
March 4, 2026
Distribution
Multiple states

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FDA Recall United States Ongoing 2026 recordClass II

Gerber Products Company dba Nestle Infant Nutrition

Product
Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged…
Reason
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
Published
March 4, 2026
Distribution
Nationwide

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FDA Recall United States Ongoing 2026 recordClass II

Pure Solutions, Inc.

Product
Pure Factors Professional Nighttime Sleep Formula and Pure F…
Reason
Label declares bovine colostrum but does not declare milk allergen.
Published
February 25, 2026
Distribution
Product was distributed to: AR, FL, CO,…

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FDA Recall United States Terminated 2026 recordClass I

Reser's Fine Foods, Inc.

Product
The Tuna Salad product container is mislabeled with a Chicke…
Reason
Undeclared fish allergen (tuna). Tuna Salad was mislabeled as Chicken Salad.
Published
February 25, 2026
Distribution
Distributed in AZ, CA, NV, UT and WA.

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FDA Recall United States Ongoing 2026 recordClass I

Lotus Mom Corporation dba Indian Kitchen Mart

Product
Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HAND…
Reason
Potential contamination with leachable lead.
Published
February 25, 2026
Distribution
U.S. Distribution: CA, CO

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FDA Recall United States Ongoing 2026 recordClass II

Lotus Mom Corporation dba Indian Kitchen Mart

Product
Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN IN…
Reason
Potential contamination with leachable lead.
Published
February 25, 2026
Distribution
U.S. Distribution: CA, CO

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FDA Recall United States Ongoing 2026 recordClass II

Lotus Mom Corporation dba Indian Kitchen Mart

Product
Brass Tope. Sticker label: $29.99+TAX
Reason
Potential contamination with leachable lead.
Published
February 25, 2026
Distribution
U.S. Distribution: CA, CO

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FDA Recall United States Ongoing 2026 recordClass II

Lotus Mom Corporation dba Indian Kitchen Mart

Product
IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label:…
Reason
Potential contamination with leachable lead.
Published
February 25, 2026
Distribution
U.S. Distribution: CA, CO

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FDA Recall United States Terminated 2026 recordClass I

Art Monkey LLC dba Why Not Natural

Product
Why Not Natural Moringa Capsules 120 capsule bottle marked w…
Reason
Potential to be contaminated with Salmonella
Published
February 25, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass I

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

by McKesson

Reason
Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.

by Meitheal Pharmaceuticals, Inc

Reason
Defective Delivery System: Missing or duplicated needles within the injection kit
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11

by Amerisource Health Services LLC

Reason
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Published
February 18, 2026
Distribution
Nationwide

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FDA Recall Ongoing 2026 recordClass II

vancomycin HCl, 2 grams, 2 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-019-59.

by Fresenius Kabi Compounding, LLC

Reason
Lack of Assurance of Sterility
Published
February 18, 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.