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Recall totals

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

37,066
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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 2,072 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)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,961–4,980 of 22,574 recalls

FDA Recall Ongoing Historical recordClass I

Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.

by Global Pharma Healthcare Private Limited

Reason
Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Dofetilide Capsules, 500 mcg (0.5 mg), 60-count bottle, Rx only, Manufactured by: Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 47335-0063-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Content Uniformity Specifications
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system) CII, 30 mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5555-3

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Out of specification for shear.
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system) CII, 20mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5554-3.

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Out of specification for shear.
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system) CII, 15 mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5553-3

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Out of specification for shear.
Published
March 29, 2023
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Daytrana (methylphenidate transdermal system) CII, 10mg, 30-count carton, Rx only, Manufactured for Noven Therapeutics, LLC., Miami by Noven Pharmaceuticals, Inc., NDC 68968-5552-3.

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: Out of specification for shear.
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

JARDIANCE (Empagliflozin), 25 mg Tablets, packaged in a) 30-count (NDC0597-0153-30) and b) 90-count (NDC 0597-0153-90) bottles, Rx only, Marketed by: Boehringer Ingelheim Pharmaceuticals, Inc. Ridgefield, CT 06877 USA and Eli Lilly and Company Indianapolis, IN 46285 USA

by Boehringer Ingelheim Pharmaceuticals, Inc.

Reason
Labeling: Label Mix-up
Published
March 29, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Sprout's Farmers Market

Product
Sprouts Farmers Market Saltine Crackers Sea Salt Tops NET WT…
Reason
Potential contamination with peanut (ingredient)
Published
March 29, 2023
Distribution
Distributors in AZ, CA, GA

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FDA Recall United States Terminated Historical recordClass III

Dollar General Corporation

Product
DG Health brand Sugar Free Daily Fiber in 10 oz. plastic con…
Reason
Product is missing warning declaration that it contains phenylalanine.
Published
March 29, 2023
Distribution
Products were distributed to the followi…

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FDA Recall United States Terminated Historical recordClass III

Titans Global Inc.

Product
WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles i…
Reason
Product was found to have milk not declared on the ingredient label
Published
March 29, 2023
Distribution
Product distributed exclusively within t…

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FDA Recall United States Terminated Historical recordClass II

Berner Foods Inc.

Product
Kirkland Signature Colombian Cold Brew Coffee ready-to-drin…
Reason
Foreign material, metal
Published
March 29, 2023
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Russell Stover Candies Inc

Product
Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4o…
Reason
Outer package is mislabeled and does not declare tree nuts (pecans).
Published
March 29, 2023
Distribution
Distributors in AL, CA, FL, GA, IN, KY,…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product
Onishi Foods Alpha Rice Matsutake Mushroom Rice 100g UPC:…
Reason
The allergen of coconut was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass I

DAISO CALIFORNIA WAREHOUSE

Product
SENNARIDO Green Snack Pistachio -Wasabi Flavor 90g UPC: 49…
Reason
The allergen of soy was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product
Kurata Menzo Meatfree Tonkotsu Ramen Dry 2P 238.8g UPC: 490…
Reason
The allergen of coconut was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product
Igarashiseimen Kitakata Spicy Umakara Ramen UPC: 496744817…
Reason
The allergen of coconut was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass I

DAISO CALIFORNIA WAREHOUSE

Product
SENNARIDO Green Snack Pistachio 90g UPC: 4974120413421 Mad…
Reason
The allergen of soy was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product
Kinjo Seika Potato Yokan 130g UPC: 4901324017056 Made in J…
Reason
The allergen of coconut was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass I

DAISO CALIFORNIA WAREHOUSE

Product
ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050111400…
Reason
The allergen of milk was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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FDA Recall United States Terminated Historical recordClass II

DAISO CALIFORNIA WAREHOUSE

Product
Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444…
Reason
The allergen of coconut was not declared on the label.
Published
March 29, 2023
Distribution
California, Washington, Nevada, Texas, N…

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.