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Recall totals

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

37,139

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 25, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small…
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: MMRF Neyyappam, UPC: 870400000111, Frozen
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: MMRF Kumbiliappam, UPC: 87040000104, Frozen
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product: Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoo…
Reason: Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product: Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Ox…
Reason: Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.

by Diamond Wipes International, Inc.

Reason: CGMP Deviations: finished products were manufactured with poor quality water.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202

by Lupin Pharmaceuticals Inc.

Reason: Superpotent Drug
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Amantadine HCl Capsules, USP, 100 mg, 50 Capsules (5x10) Unite Dose, Rx Only, Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-069-15

by AVKARE Inc.

Reason: Failed Dissolution Specifications
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.

by Sandoz Incorporated

Reason: Cross Contamination With Other Products: presence of unrelated ingredients (i.e. traces of Lisinopril, Mannitol, Iron, Calcium and Phosphorous).
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

WipeEssentials Wet Wipes (benzalkonium chloride 0.13%), 30-count pouches, Dist. by Diamond Wipes Int'l, Inc., Chino, CA 91710, UPC 7 66670 03988 6.

by Diamond Wipes International, Inc.

Reason: CGMP Deviations: finished products were manufactured with poor quality water.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches Rx Only NDC 68968-5552-3 Manufactured for Noven Therapeutics, LLC., Miami, FL 33186 by Noven Pharmaceuticals, Inc. Miami, FL 33186 1-877-567-7857

by Noven Pharmaceuticals, Inc.

Reason: Defective Delivery System: Out of specification for adhesive transfer.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Pain Out Thai Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Pain Out Maeng Da Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Pain Out Green Malay Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Nirvanio Special Reserve Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Nirvanio Maeng Da Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Nirvanio Green Malay Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Nirvanio Bali Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutrizone LLC

Product: Cali Thai Kratom all packages, all quantities
Reason: Dietary supplements have the potential to be contaminated with Salmonella.
Published: April 25, 2018
Distribution: Nationwide

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Data last updated: September 25, 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.