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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 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 20,280 recalls

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

Oregon Potato Company

Product
IQF 3/8" Un-Blanched Yellow Onion Dice, Frozen, item number…
Reason
IQF 3/8" Un-Blanched, Frozen, Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
IQF 3/4" Yellow Onion Dice, Frozen, item number 101430, bulk…
Reason
IQF 3/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
IQF 3/8" Yellow Onion Strip, Frozen, Item number 103331, bul…
Reason
IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip are voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
3/8" White Onion Dice- FRESH, item number 105197, bulk tote,…
Reason
3/8" White Onion Dice- FRESH is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
IQF 1/4" Yellow Onion Dice, frozen, item numbers: 103364, 10…
Reason
IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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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

Oregon Potato Company

Product
705000 IQF 3/8" Dice Yellow Onion, item number 101472, bulk…
Reason
3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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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 I

Oregon Potato Company

Product
IQF 1/4" Frozen WHITE Onion Dice, item number 103342, bulk c…
Reason
IQF 1/4" White Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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FDA Recall United States Terminated Historical recordClass I

Greenland Trading Corp

Product
Al Rasheed Sardine Item #4017 Label not available - NYSDAM…
Reason
Greenland Trading Corporation is recalling Al Rasheed Sardines due to potential C. botulinum contamination.
Published
August 24, 2016
Distribution
CA, FL, MA, NJ, NY, PA and TN

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FDA Recall United States Terminated Historical recordClass I

Oregon Potato Company

Product
3/8" White Onion Strip-FRESH, item number 105196, bulk totes…
Reason
3/8" White Onion Strip-FRESH was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Published
August 24, 2016
Distribution
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ,…

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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

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.