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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 October 2026.

37,206
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 15,681–15,700 of 20,441 recalls

FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-123-90, Rx Only, GSMS.

by Golden State Medical Supply Inc.

Reason
Failed Dissolution Specifications: Out-of-specification results in retained sample.
Published
August 24, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glipizide 2.5 mg Extended-release tablets, 30-count bottle, Rx Only, Manufactured By: Patheon Pharmaceuticals Inc Cincinnati, OH 45237, NDC 00591-0900-30

by Actavis Inc

Reason
Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Domino Foods, Inc.

Product
Domino PURE CANE LARGE GRAIN GRANULATED SUGAR, NET WT 50 LB…
Reason
Product was found to contain metal fragments.
Published
August 24, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

HELLOFRESH

Product
Summer Vegetable Salad with Seared Chicken, Garlic Croutons,…
Reason
Possible contamination with Listeria monocytogenes
Published
August 24, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

HELLOFRESH

Product
Nir's Lamb-Stuffed Zucchini with Spiced Lentil Stew
Reason
Possible contamination with Listeria monocytogenes
Published
August 24, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Kerry, Inc

Product
Golden Dipt¿ Jalape¿o Breader is in a white 10 pound bag wit…
Reason
Kerry Inc. was notified by our supplier that two of their products, a red bell pepper nugget and a jalapeno nugget, were made with a small percentage of affected flour which was recalled by General Mills because it may be contaminated with E. coli O121.
Published
August 24, 2016
Distribution
FL IL KS MI MN MO NJ OK TX CANA…

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FDA Recall United States Terminated Historical recordClass I

HELLOFRESH

Product
Seared Steak with Spring Veggie Succotash and Mint-Chive Pes…
Reason
Possible contamination with Listeria monocytogenes
Published
August 24, 2016
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Newly Weds Foods Inc

Product
Bulk flour bland breader packaged into 15, 30, and 50 lb bag…
Reason
Flour contaminated with E. coli O121 was used in the manufacuring of flour based blends.
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Kerry, Inc

Product
SOUTHWEST BREADER G2293 25 LB BAG POLY BAG ITEM G2293.43
Reason
Kerry Inc. was notified by our supplier that two of their products, a red bell pepper nugget and a jalapeno nugget, were made with a small percentage of affected flour which was recalled by General Mills because it may be contaminated with E. coli O121.
Published
August 24, 2016
Distribution
FL IL KS MI MN MO NJ OK TX CANA…

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FDA Recall United States Terminated Historical recordClass I

HELLOFRESH

Product
Lemony Pan-Seared Chicken with Pesto Potato Salad and Peas
Reason
Possible contamination with Listeria monocytogenes
Published
August 24, 2016
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0093-0661-16

by Teva North America

Reason
Presence of Foreign Substance; presence of black particles describes generically as cellulose-based bundles of brown fibrous material.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Chicken Patty Sandwich Chicken Pat…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Submarine on a French Roll Turkey…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Cafe Favorites Oven Roasted Turkey Breast Sub Code #C02284…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Turkey Ham & Cheese Sandwich on a…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Turkey Bologna & Cheese Sandwich T…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Cafe Favorites Turkey Ham & Cheese Deli Flatz Code #C22148…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service All American Cheese Burger Beef Pa…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Cafe Favorites Turkey Sausage & Cheese Sunrise Twist Code…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Let's Do Lunch, Inc.

Product
Integrated Food Service Turkey Ham & Cheese Sandwich on a…
Reason
Potential Listeria monocytogenes contamination.
Published
August 17, 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.