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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.

37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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)

  • 1,527 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 8,641–8,660 of 20,769 recalls

FDA Recall United States Terminated Historical recordClass I

Blendtopia Products, LLC

Product
Blendtopia Superfood Smoothie Kit Energy flavor, 7 oz flexib…
Reason
Potential contamination of Listeria monocytogenes.
Published
March 11, 2020
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Blendtopia Products, LLC

Product
Blendtopia Superfood Smoothie Kit Strength flavor, 7 oz flex…
Reason
Potential contamination of Listeria monocytogenes.
Published
March 11, 2020
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Blendtopia Products, LLC

Product
Blendtopia Superfood Smoothie Kit Immunity flavor, 7 oz flex…
Reason
Potential contamination of Listeria monocytogenes.
Published
March 11, 2020
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Blendtopia Products, LLC

Product
Blendtopia Superfood Smoothie Kit Detox flavor, 7 oz flexibl…
Reason
Potential contamination of Listeria monocytogenes.
Published
March 11, 2020
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

Blendtopia Products, LLC

Product
Blendtopia Superfood Smoothie Kit Glow flavor, 7 oz flexible…
Reason
Potential contamination of Listeria monocytogenes.
Published
March 11, 2020
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL), Solution for Intravenous Infusion, Sterile Solution, 100 mL Single - Dose Vial per Carton, Rx Only, Distributed by: Breckenridge Pharmaceutical, Inc., Boca Raton, FL 33487, Manufactured by: Pharmaceutics International, Inc., Hunt Valley, MD 21031, NDC 51991-064-98.

by Breckenridge Pharmaceutical, Inc

Reason
Failed Impurities/Degradation Specifications: Out-of-specification results obtained for impurities during stability testing.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Phenytoin Oral Suspension USP, 125 mg/5 mL potency, 8 fl oz (237 mL) Rx Only Mfd. by: Taro Pharmaceuticals Industries Ltd. Haifa Bay, Israel 2624761 Dist. by: Taro Pharmaceuticals U.S.A. Inc. Hawthorne, NY 10532, NDC 51672-4069-1

by Taro Pharmaceuticals U.S.A., Inc.

Reason
Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL may coagulate and may not resuspend as per the label copy instructions.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

CVS Health Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed By: CVS Pharmacy Inc. One CVS Drive, Woonsocket, RI 02895, NDC 59779-303-01

by Akorn, Inc.

Reason
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the tube.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Well at Walgreens Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015. NDC 0363-9050-00.

by Akorn, Inc.

Reason
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the tube.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Sodium Chloride Ophthalmic Ointment USP, 5%, 3.5 g tubes, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-622-35

by Akorn, Inc.

Reason
Presence of Particulate Matter: Brown spots observed on the inside of the tube of product, identified as tin with trace copper, which are the base of the materials of construction for the tube.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

TRAMADOL HYDROCHLORIDE Tablets, USP, 50 mg, Rx Only a)100-count bottles (NDC 60429-588-01) b) 500-count bottle (NDC 60429-588-05) Manufactured by Teva Czech Industries, s.r.o. Opava-Komarov, Czech Republic, Packaged by GSMS Incorporated, Camarillo, CA 93012

by Golden State Medical Supply Inc.

Reason
Labeling: Incorrect package insert - Patient leaflets for the specified lots of unscored tablets contain language relative to a 25 mg dosing titration that necessitates the use of a scored 50 mg tablet.
Published
March 4, 2020
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Coburn Farms Snackers, Sharp Yellow Cheddar Cheese, Cherry J…
Reason
Coburn Farms 4.5oz Snackers is being recalled due to a labeling error leading to undeclared peanut.
Published
March 4, 2020
Distribution
Save-A-Lot Retail Stores located in FL,…

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FDA Recall United States Terminated Historical recordClass II

Sierra Soups

Product
Sierra Soups Pasta e Fagioli: All Natural Vegetarian Vega…
Reason
Firm was notified that their Gluten Free Soup mix labeling is misleading as pasta containing wheat is an ingredient.
Published
March 4, 2020
Distribution
US - CA, MA, NY, WI

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FDA Recall United States Terminated Historical recordClass II

CJ Foods Inc., A Division of CJ America

Product
Annie Chun's Japanese Style Teriyaki Noodle Bowl with Cooked…
Reason
Pad Thai Noodle Bowl which contains peanuts was packaged with the sleeve for Teriyaki Noodle Bowl leaving undeclared peanuts on the product label.
Published
March 4, 2020
Distribution
WA, RI, CA, FL, TN, PA, MN, IL, WI, and…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
SYSCO Classic Light Brown Cane Sugar, 25 LB bag, UPC 0748659…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
SYSCO Classic Light Brown Cane Sugar, 32 oz (2 LB) plastic b…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
HY-VEE Pure Cane Light Brown Sugar, 32 oz (2 LB) plastic bag…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
Great Value Light Brown Sugar, 32 oz (2 LB) plastic bag, UPC…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
Domino Premium Pure Cane Medium Brown Sugar, 50 LB bag, UPC…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Domino Foods Inc

Product
Domino Premium Pure Cane Golden Light Brown Sugar, 50 LB bag…
Reason
Possible foreign material.
Published
March 4, 2020
Distribution
Product was shipped to the following sta…

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.