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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass III

Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505, NDC 51079-882-20

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Impurities/Degradation Specifications: out of specification result for Clonazepam Related Compound (RC) A (a known impurity) at 16 month timepoint.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clonazepam Tablets, USP, 0.5 mg, packaged in a)100- count unit dose box of 10 x 10 blister cards (NDC 51079-881-20) and b) 300-count unit dose box of 10 x 30 punch cards (NDC 51079-881-56), Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Impurities/Degradation Specifications: out of specification result for Clonazepam Related Compound (RC) A (a known impurity) at 15 month timepoint.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM - Kamedis Bio-Herbal Dandruff Care 0.1% PYRITHIONE ZINC, STEP 1 PRE-TREAT Concentrated Botanical Scalp Lotion (0.1% Pyrithione Zinc) 4.20 FL OZ (125mL) (NDC 51672-2126-0) and STEP 2 CLEANSE Concentrated Botanical Dandruff Shampoo (1.0% Pyrithione Zinc)(0.6.80 FL OZ (200 mL) (NDC 51672-2125-5), Distributed by: Taro Pharmaceuticals U.S.A, Inc. Hawthorne, NY 10532. NDC

by Taro Pharmaceuticals U.S.A., Inc.

Reason: Subpotent Drug: Out of Specification assay values on stability for the active ingredient, zinc pyrithione.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms Michigan Cherry Preserves 12oz glass bottle…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms Strawberry Preserves 12oz glass bottles and…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms America's Original Cherry Butter 12oz and…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms Jalapeno Cherry Butter 12oz and 20oz glass…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms Pear & Cinnamon Preserves 10oz glass bottle…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Brownwood Farms

Product: Brownwood Farms Cherry Raspberry Preserves 12oz glass bottl…
Reason: Products contain milk not declared on the label.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

The Hershey Company

Product: SOFiT Protein Plus Pumpkin Seeds Sesame Garlic, Seeds covere…
Reason: The Hershey Company has issued a voluntary recall of three products sold under the SoFit brand after a supplier who provides sunflower seeds for the products expanded its recall on June 1. Products have the potential to be contaminated with Listeria monocytogenes.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

The Hershey Company

Product: SOFiT Protein Plus Almonds Jalapeno Garlic, whole almonds co…
Reason: The Hershey Company has issued a voluntary recall of three products sold under the SoFit brand after a supplier who provides sunflower seeds for the products expanded its recall on June 1. Products have the potential to be contaminated with Listeria monocytogenes.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

The Hershey Company

Product: SOFiT Protein Plus Sunflower Seeds Sea Salt; Seeds covered b…
Reason: The Hershey Company has issued a voluntary recall of three products sold under the SoFit brand after a supplier who provides sunflower seeds for the products expanded its recall on June 1. Products have the potential to be contaminated with Listeria monocytogenes.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Professional Botanicals

Product: Professional Botanicals MealPlex (756 grams) and Veo Natural…
Reason: Professional Botanicals announces a voluntary field action for MealPlex and Pearl due to undeclared milk allergen.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Rich Products Corp

Product: New York Style Chocolate Iced ¿clairs under the following la…
Reason: Products were recalled due to the potential presence of plastic foreign material.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Truco Enterprises, Inc

Product: On the Border Blue Corn Tortilla Chips 7.25 oz. and 10 oz. p…
Reason: Possible metal fragments in corn flour.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Truco Enterprises, Inc

Product: On the Border Cafe Style Tortilla Chips 18 oz. and 28 oz. pa…
Reason: Possible metal fragments in corn flour.
Published: November 16, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride, 20 mg per mL, 200 mg per 10 mL, 10 mL vials, Rx only, PharMEDium Services, LLC, Memphis, TN, NDC 61553-0364-65.

by PharMEDium Services, LLC

Reason: Lack of Assurance of Sterility: A portion of the batch quantity was compounded outside of the firm's process media validation.
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC 17478-623-12.

by Akorn Inc

Reason: Subpotent Drug: concentration of product is less than labeled amount.
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

Gildess 24 FE 1.5/30 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, (a) 3 blisters (NDC 0603-7610-49), and (b) 6 blisters (NDC 0603-7610-17), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811

by Par Pharmaceutical, Inc.

Reason: Subpotent Drug; Ethinyl Estradiol
Published: November 9, 2016
Distribution: Nationwide

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FDA Recall Completed Historical recordClass III

Gildess FE 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP and ferrous fumarate tablets, USP 75 mg), 6 blisters (28 count), NDC 0603-7608-17, Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST PHARMACEUTICALS, USA, Huntsville, AL 35811

by Par Pharmaceutical, Inc.

Reason: Subpotent Drug; Ethinyl Estradiol
Published: November 9, 2016
Distribution: Nationwide

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Data last updated: September 30, 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.