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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).
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 13,341–13,360 of 18,130 recalls

FDA Recall United States Terminated Historical recordClass II

La Torre Foods Usa, Inc.

Product
la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz…
Reason
Calcium caseinate is declared on the label, but milk is not listed.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Montana Flour & Grains, Inc

Product
100% Organic Spelt Flour, packaged in 10 lbs., 25 lbs. and…
Reason
Organic Spelt Flour is recalled because label does not declare wheat.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Montana Flour & Grains, Inc

Product
100% Organic Unbleached White Flour, packaged in 10 lbs., 2…
Reason
Organic Unbleached White Flour is recalled because label does not declare wheat.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Montana Flour & Grains, Inc

Product
100% Organic Spelt Grain, packaged in 10 lbs., 25 lbs. and…
Reason
Organic Spelt Grain is recalled because label does not declare wheat.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles (NDC 68382-035-16), and c) 1000-count bottles, (NDC 68382-035-10), Rx only, Manufactured by : Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications: out of specification dissolution results in retained samples
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine HCL ER Capsule USP, 150mg, packaged in a) 30-count bottles (NDC 68382-036-06), b) 90-count bottles (NDC 68382-036-16), and c) 1000-count bottles, (NDC 68382-036-10), Rx only, Manufactured by : Cadila Healthcare Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications: out of specification dissolution results in retained samples
Published
August 24, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90

by Golden State Medical Supply Inc.

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

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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

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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 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 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.