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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.

37,142
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 12,301–12,320 of 19,943 recalls

FDA Recall United States Terminated Historical recordClass I

Health Matters America Inc.

Product
Organic traditions brand DARK CHOCOLATE HAZELNUTS WITH CHILI…
Reason
The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published
December 13, 2017
Distribution
Retail stores located in Arizona, Califo…

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FDA Recall United States Terminated Historical recordClass I

Health Matters America Inc.

Product
Organic traditions brand DARK CHOCOLATE HAZELNUTS, NET WT.…
Reason
The imported products were found to contain undeclared milk (casein) based on analyses by the Canadian Food Inspection Agency (CFIA).
Published
December 13, 2017
Distribution
Retail stores located in Arizona, Califo…

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FDA Recall Terminated Historical recordClass II

Paroxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 count (NDC 68382-099-10) count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534

by Zydus Pharmaceuticals USA Inc

Reason
Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Published
December 6, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC 8 94140 00103 0.

by EAI-JR286 INC

Reason
CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not limited to failed viscosity.
Published
December 6, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC 0574-0222-01

by Mayne Pharma Inc

Reason
Failed Dissolution Specifications.
Published
December 6, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Goa 403 722 India, NDC 68180-295-06, UPC 368180295068

by Lupin Pharmaceuticals Inc.

Reason
Failed Dissolution Specification
Published
December 6, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICALS IND, LTD, Jerusalem Israel, Manufactured For: TEVA PHARMACEUTICALS USA, North Wales, PA, NDC 00093-7772-05

by Teva Pharmaceuticals USA

Reason
Failed Tablet/Capsule Specifications; potential presence of broken tablets.
Published
December 6, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Elevation Brands, LLC

Product
Ian's Gluten Free Italian Breadcrumbs, UPC# 7-49512-77660-6
Reason
Product may have been exposed to beetles from a raw material supplier. There were no actual findings of insects in any finished product.
Published
December 6, 2017
Distribution
Wholesale Distribution in the following…

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FDA Recall United States Terminated Historical recordClass III

Elevation Brands, LLC

Product
Ian's Gluten Free Original Panko Breadcrumbs, UPC# 7-49512-7…
Reason
Product may have been exposed to beetles from a raw material supplier. There were no actual findings of insects in any finished product.
Published
December 6, 2017
Distribution
Wholesale Distribution in the following…

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FDA Recall United States Terminated Historical recordClass II

Reese Pharmaceutical Company

Product
Orange Flavor Immune Support Dietary Supplement Effervescent…
Reason
The label does not list "Sodium" in the ingredient statement.
Published
December 6, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Reese Pharmaceutical Company

Product
Berry Flavor Immune Support Dietary Supplement Effervescent…
Reason
The label does not list "Sodium" in the ingredient statement.
Published
December 6, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

Pure Encapsulations, Inc.

Product
pure encapsulations AI Enzymes DIETARY SUPPLEMENT 120 CAPSUL…
Reason
Product contains undeclared sulfites.
Published
December 6, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Pure Encapsulations, Inc.

Product
Pure Encapsulations Systemic Enzyme Complex DIETARY SUPPLEME…
Reason
Product contains undeclared sulfites.
Published
December 6, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Dutch Valley Food Distributors Inc.

Product
Dark Chocolate Cashew, Net 11 oz., Contains Cashew and Soy,…
Reason
Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
Published
December 6, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Dutch Valley Food Distributors Inc.

Product
Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy,…
Reason
Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
Published
December 6, 2017
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

Dexamethasone Sodium Phosphate Injection, USP, 20 mg/5 mL (4 mg/mL), 5 mL Vials (NDC 0641-6146-01), packaged in 25 x 5 mL Vials per shelf pack (NDC 0641-6146-25), Rx Only, Manufactured by WEST-WARD, Eatontown, NJ 07724 USA.

by West-Ward Pharmaceuticals Corp.

Reason
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Vials (NDC 0641-6145-01), packaged in 25 x 1 mL Vials per shelf pack (NDC 0641-6145-25), Rx Only, Manufactured by WEST-WARD, Eatontown, NJ 07724 USA.

by West-Ward Pharmaceuticals Corp.

Reason
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Columbus, Ohio 43217, NDC 68084-046-01

by Amerisource Health Services

Reason
Presence of Foreign Tablets/Capsules.
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lorazepam Tablets, USP CIV, 0.5 mg, 500-count bottle, Rx Only, Manufactured by: Leading Pharma, LLC Fairfield, NJ 07004 NDC 69315-904-05

by Leading Pharma, LLC

Reason
Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, Unsalted European Style Butter Blend Margarine (169…
Reason
SunGlow contains undeclared soy lecithin.
Published
November 29, 2017
Distribution
Multiple states

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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.