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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 14,461–14,480 of 19,220 recalls

FDA Recall Terminated Historical recordClass II

Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505; Packaged and Distributed By: UDL Laboratories, Inc., Rockford, IL 61103.

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason
CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Urea (50% Urea in a Cream Base), a) Net Wt. 5 oz (142 g), (NDC 42808-0200-05) b) Net Wt. 9 oz (225 g) (NDC 42808-0200-09), Rx Only, Manufactured in the U.S.A. for Exact-Rx Inc., Melville, NY

by Exact-Rx Inc

Reason
Crystallization; complaints received by the manufacturer of crystals forming in product
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Remeven Cream, (50% Urea in a Cream Base), a) 5.0 oz (142 g) and b) 9.0 oz (255 g) tubes, Rx only, Manufactured by Sonar Products Inc, Carlstadt, NJ. Distributed by Stratus Pharmaceuticals Inc., Miami, FL.

by Stratus Pharmaceuticals Inc

Reason
Crystallization; Complaints that cream appears to have crystallized
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection, 12 mg, 10 ml depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247

by Talon Compounding Pharmacy

Reason
Lack of Assurance of Sterility
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Human Chorionic Gonadotropin Injection (a) 2500 iu, (b) 2500 iu with B12, (c) 3500 iu, (d) 5000 iu, (e) 5000 iu with B12, (f) 6000 iu, (g) 7500 iu, (h) 7500 iu with B12, (i)11,000 iu, (j)11,000 iu with B12, (k) 15,000 iu, (l) 20,000 iu, (m) 20,000 iu with B12, 10 mL sterile, depyrogenated vials, Rx Only, Compounded by Talon Compounding Pharmacy, San Antonio, TX 78247

by Talon Compounding Pharmacy

Reason
Lack of Assurance of Sterility
Published
August 31, 2016
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mondelez International

Product
Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Graham Snack…
Reason
Teddy Graham Cub Snacks were produced using Grain Craft Flour containing peanut residue.
Published
August 31, 2016
Distribution
Nationwide

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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

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,…

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.