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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.

37,139
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 2,072 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)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 10,801–10,820 of 18,028 recalls

FDA Recall Terminated Historical recordClass II

Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Columbus, Ohio 43217, NDC 68084-046-01

by Amerisource Health Services

Reason
Presence of Foreign Tablets/Capsules.
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lorazepam Tablets, USP CIV, 0.5 mg, 500-count bottle, Rx Only, Manufactured by: Leading Pharma, LLC Fairfield, NJ 07004 NDC 69315-904-05

by Leading Pharma, LLC

Reason
Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam
Published
November 29, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
SunGlow, Unsalted European Style Butter Blend Margarine (169…
Reason
SunGlow contains undeclared soy lecithin.
Published
November 29, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Shoreline Fruit, LLC

Product
Shoreline Fruit Dark Choc Covered Montmorency Cherries packa…
Reason
Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.
Published
November 29, 2017
Distribution
Domestic: AK AL AR AZ CA CO CT DC…

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FDA Recall United States Terminated Historical recordClass II

Shoreline Fruit, LLC

Product
Dried Dark Chocolate Covered Cherries, The products are pack…
Reason
Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.
Published
November 29, 2017
Distribution
Domestic: AK AL AR AZ CA CO CT DC…

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FDA Recall Terminated Historical recordClass III

Meclizine hydrochloride tablets USP, 12.5 mg, 100 count HDPE bottle, Rx only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-122-06

by Jubilant Cadista Pharmaceuticals, Inc.

Reason
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3) and d) 100 G bottle (NDC 51552-1392-5), Rx only, Distributed by Fagron, Inc., 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel. 1-(800) 423-6967

by Fagron, Inc

Reason
cGMP Deviations: lack of quality assurance at the API manufacturer.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Lumigan (bimatoprost ophthalmic solution) 0.01%, 2.5 mL bottle, Rx only, Allergan, Irvine, CA 92612. NDC# 0023-3205-03

by Allergan Sales, LLC

Reason
Failed Impurities/Degradation Specifications.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC# 0023-9211-03; b) 5 mL (NDC# 0023-9211-05); c) 10 mL (NDC# 0023-9211-10); d) 15 mL (NDC# 0023-9211-15) bottles, Manufactured By: Allergan, Irvine, CA 92612..

by Allergan Sales, LLC

Reason
Failed Impurities/Degradation Specifications.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection, for intravenous use, Rx Only, Mfd. by: Teva Pharmachemie Swensweg 5 Haarlem, The Netherlands Mfd. for: Genzyme Corporation, Cambridge, MA 02142, NDC 0024-5860-01.

by Genzyme Corporation

Reason
Labeling: Incorrect or Missing Package Insert.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC: 68084-390-01

by Amerisource Health Services

Reason
Failed Stability Specifications
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

doTERRA International, LLC

Product
Slim & Sassy¿ TrimShake Chocolate, SKU 35200001, 1 lb 5.9…
Reason
doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake - Chocolate and Slim & Sassy¿ TrimShake Vanilla mixes due to an undeclared milk allergen.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Setton International Foods Inc

Product
(1) Setton Farms Deluxe Dark Chocolate Raisins 24oz. plastic…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
CT, MA, ME, NH, NY, PA, and VT.

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FDA Recall United States Terminated Historical recordClass II

Setton International Foods Inc

Product
(1)Setton Farms Deluxe Dark Chocolate Almonds 20oz. plastic…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
CT, MA, ME, NH, NY, PA, and VT.

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FDA Recall United States Terminated Historical recordClass I

doTERRA International, LLC

Product
Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz,…
Reason
doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake - Chocolate and Slim & Sassy¿ TrimShake Vanilla mixes due to an undeclared milk allergen.
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in :…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Coffee beans packaged in Bulk 4 oz. Plasti…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Pl…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz.…
Reason
Product contains undeclared milk
Published
November 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product
Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch,…
Reason
Product contains undeclared milk
Published
November 22, 2017
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.