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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
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

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 15,521–15,540 of 20,968 recalls

FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Hostess Ding Dongs, chocolate cake with creamy filing, packa…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass I

SunOpta Food and Grain, Inc.

Product
2nd EXPANSION 5/31/2016 Navitas Naturals, Superfood HEMP,…
Reason
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016
Published
September 21, 2016
Distribution
AR, CA, CO, IL, IN, KY, MN, NC, ND, NH,…

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Iced Vanilla cake with creamy filling, packaged as Hostess Z…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Hostess Donettes Powdered Mini Donuts, packaged in 9ct and 6…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Ultimate Nutrition, Inc.

Product
ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Di…
Reason
Product contains undeclared milk.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Completed Historical recordClass I

SunOpta Food and Grain, Inc.

Product
2nd EXPANSION 5/31/2016 Product shipped OUS only. Spitz Di…
Reason
SunOpta is recalling sunflower kernel products that have the potential to be contaminated with Listeria monocytogenes. EXPANDED 5/18/2016 SunOpta expanded their recall of roasted sunflower kernel products to include the production dates of February 20 - April 26, 2016 due to potential Listeria monocytogenes contamination. 2nd EXPANSION 5/31/2016 SunOpta expanded their recall to include product produced at their Crookston, MN facility, still within expiry, to include the production dates of May 31, 2015 thru January 31, 2016
Published
September 21, 2016
Distribution
AR, CA, CO, IL, IN, KY, MN, NC, ND, NH,…

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Chocolate Frosted Mini Donuts, packaged in 6-20ct and 9ct ba…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mars Chocolate North America

Product
COMBOS CHEDDAR CHEESE CRACKER - Net Wt. 6.30 oz (178.6 g) Ma…
Reason
Mars Chocolate North America is recalling select Combos due to the potential for undeclared peanut residue.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Hostess Donettes Maple Glazed Mini Donuts, packaged in 9-17-…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Hostess Brands, LLC

Product
Hostess Chocodile Twinkies, chocolate covered sponge cake wi…
Reason
Product is manufactured with flour known to contain peanut allergen and is not labeled to contain peanuts.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

The Pictsweet Company

Product
Pictsweet(R) Seasoned Summer Vegetables, NET WT 12 OZ. (340g…
Reason
Possible Listeria Monocytogenes contamination in bulk vegetables supplied by CRF Frozen Foods, LLC used in manufacturing several Pictsweet products.
Published
September 21, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate Injection, USP, 50 mg/mL, Single Dose Vial, packaged in a) 1 mL fill in a 2 mL Vial (NDC: 69053-008-01); and b) 25 x 2 mL Vials (NDC 69053-008-02), Rx only, Manufactured for: Andersen Pharmaceutical, White Plains, NY 10605.

by Allergy Laboratories, Inc.

Reason
Lack of Assurance of Sterility: An FDA inspection at the facility raised concerns that product sterility was potentially impacted.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Ondansetron Injection USP 40 mg/20 mL (2 mg/mL), Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454 NDC # 0703-7226-01 (20 mL- Multi-dose Vial), NDC # 0703-72263-03 (10 Multi-dose Vials per carton)

by Teva North America

Reason
CGMP Deviations
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial, For Intravenous Use Only, Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-1179-01.

by Teva North America

Reason
CGMP Deviations
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Linezolid Injection 600 mg/300 mL Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-9060-31- (Single Use Container), NDC# 0703-9060-33 (Box of 10 Singe Use Containers)

by Teva North America

Reason
CGMP Deviations
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-0020-31 (Single Use Bag), NDC # 0703-0020-32 (5 Single Use Bags in One Carton).

by Teva North America

Reason
CGMP Deviations
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Bromocriptine Mesylate Capsules USP, 5 mg, 30-count bottles, Rx only, Manufactured by: Cadila Healthcare ltd., Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534, NDC 68382-110-06

by Zydus Pharmaceuticals USA Inc

Reason
Failed impurities/degradation specifications: Out of specification results noticed in related substance test during analysis of 24 months long term (25 degree Celsius /65% RH) stability samples of two batches.
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 30 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-887-32; Blister NDC 68084-887-33

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules CII 25 mg 20 UD Capsules (5 x 4), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH ---- Carton NDC 68084-909-32; Blister NDC 68084-909-33

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate (Mixed Salts of a Single-Entity Amphetamine Product) Extended-Release Capsules, CII 20 mg, 30 UD Capsules (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus, OH --- Carton NDC 68084-832-25; Blister NDC 68084-832-95

by Amerisource Health Services

Reason
Unit Dose Mispackaging; blister cavities may contain more than one tablet /capsule
Published
September 14, 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.