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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.

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
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)

  • 1,714 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).
  • Oct 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 II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 16,721–16,740 of 22,189 recalls

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 II

1 Epic, LLC

Product
Fruit 66 Passion Fruit Mango, 8 FL OZ (240 mL) 100% Juice No…
Reason
1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice products because the cans are experiencing swelling that can cause the lids of the can to pop off and potentially cause an injury.
Published
November 16, 2016
Distribution
AL, CA, FL, GA, IL, KY, MD, MI, NY, OH,…

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FDA Recall United States Terminated Historical recordClass II

1 Epic, LLC

Product
Fruit 66 Tropical Punch, 8 FL OZ (240 mL) 100% Juice Non-Car…
Reason
1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice products because the cans are experiencing swelling that can cause the lids of the can to pop off and potentially cause an injury.
Published
November 16, 2016
Distribution
AL, CA, FL, GA, IL, KY, MD, MI, NY, OH,…

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FDA Recall United States Terminated Historical recordClass II

1 Epic, LLC

Product
Fruit 66 Strawberry Melon, 8 FL OZ (240 mL) 100% Juice Non-C…
Reason
1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice products because the cans are experiencing swelling that can cause the lids of the can to pop off and potentially cause an injury.
Published
November 16, 2016
Distribution
AL, CA, FL, GA, IL, KY, MD, MI, NY, OH,…

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FDA Recall United States Terminated Historical recordClass II

1 Epic, LLC

Product
Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbon…
Reason
1 Epic is recalling specific lots of various Fruit 66 100% Fruit Juice products because the cans are experiencing swelling that can cause the lids of the can to pop off and potentially cause an injury.
Published
November 16, 2016
Distribution
AL, CA, FL, GA, IL, KY, MD, MI, NY, OH,…

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FDA Recall United States Terminated Historical recordClass II

Kar Nut Products Company

Product
Fit & Active 100 Calorie Whole Almonds 7  0.63oz bags per…
Reason
Walnuts undeclared on outer retail unit carton.
Published
November 16, 2016
Distribution
PA KS MI IL NC OH CT

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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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FDA Recall Completed Historical recordClass III

Gildess FE 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, 6 blisters (NDC 0603-7609-17), 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 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0,02 mg, USP), 21 count, (a) 3 blisters (NDC 0603-7607-48) and (b) 6 blisters (NDC 0603-7607-15), 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

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.