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Recall totals

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

37,324

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

State: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 21, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Pickled Radish distributed in un-labeled plastic co…
Reason: Seasoned Pickled Radish was recalled due to undeclared wheat, sesame, and Y5.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall OngoingHistorical 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 TerminatedTerminated: October 18, 2023Historical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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

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FDA Recall OngoingHistorical 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 TerminatedTerminated: December 4, 2023Historical 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 TerminatedTerminated: August 18, 2023Historical 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 TerminatedTerminated: February 23, 2024Historical 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 TerminatedTerminated: March 23, 2023Historical recordClass II

4 J's Treats, LLC dba Bruttles Gourmet Candies

Product: Butter Toffee, net wt. 16 oz, 6 units per case. Label declar…
Reason: The Butter Toffee, 16oz box, declares butter but does not declare milk. Label does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays. The Butter Toffee, 4oz part of the SAMPLERS package, declares butter but does not declare milk, and it does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays.
Published: March 29, 2023
Distribution: distributed in Washington

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FDA Recall United States TerminatedTerminated: June 28, 2023Historical recordClass II

BA Sports Nutrition, LLC

Product: BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Lite…
Reason: Potential for plastic pieces in product
Published: March 29, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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 TerminatedTerminated: May 3, 2024Historical 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…

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Data last updated: October 21, 2026 ET

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.