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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

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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 13,801–13,820 of 18,130 recalls

FDA Recall United States Terminated Historical recordClass I

Dr. Praeger'S Sensible Foods

Product
Dr. Praeger's Tex Mex Veggie Burgers, 6 x 10 oz. (283g)/box,…
Reason
Dr. Praeger's Sensible Food/Ungar's Food Products is voluntarily recalling various not-ready-to eat frozen products because they may be contaminated with Listeria monocytogenes.
Published
July 20, 2016
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Dr. Praeger'S Sensible Foods

Product
Ungar's Veggie Balls (Vegan), 1 oz., 10 lbs (4.54 kg), Best…
Reason
Dr. Praeger's Sensible Food/Ungar's Food Products is voluntarily recalling various not-ready-to eat frozen products because they may be contaminated with Listeria monocytogenes.
Published
July 20, 2016
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass I

Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180

by XTREME Z DISTRIBUTORS INC

Reason
Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed the presence of sibutramine and desmethylsibutramine.
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

MIDAZOLAM HCl in 0.9% Sodium Chloride Injection, 2 mg/2 mL (1 mg/mL), in 2 mL syringe, Rx only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-001-16 UPC: 0100352533001161

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

MIDAZolam HCl 0.1 mg/mL in 5% DEXTROSE 2.5 mL syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999993721

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Midazolam HCl in 0.9% Sodium Chloride Injection, 0.5 mg/mL 1 mL (0.5 mg/mL), 1 mL syringes, Rx Only, Cantrell Drug Co., Little Rock AR --- NDC 52533-157-45, UPC: 0100352533157455

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection, packaged in 3 mL Syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992033

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HEPARIN Sodium in 0.45% Sodium Chloride, 1 USP Unit/2 mL (0.5 USP Units/mL), Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-148-16, UPC: 0100352533148163

by Cantrell Drug Company

Reason
Stability Data Does Not Support Expiry
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HEParin Sodium 0.5 USP UNITS/mL in 0.225% SODIUM CHLORIDE, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992212

by Cantrell Drug Company

Reason
Stability Data Does Not Support Expiry
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection, packaged in 2 mL syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-074-16, UPC: 0100352533074165

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection, in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999993491

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection, in 2 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock AR --- UPC: 9999993301

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

fentaNYL Citrate 1 MCG/mL in 0.9% Sodium Chloride Injection, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992131

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

fentaNYL citrate in 0.9% Sodium Chloride Injection, 10 mcg/1 mL (10 mcg/mL), in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-024-45, UPC: 0100352533024450

by Cantrell Drug Company

Reason
Subpotent Drug
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles

by Bee Extremely Amazed LLC

Reason
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

XCEL ADVANCED Capsules, 350mg, 60-count bottles, Manufactured for JNS Health

by Bee Extremely Amazed LLC

Reason
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health

by Bee Extremely Amazed LLC

Reason
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared fluoxetine, an FDA approved drug used to treat depression, anxiety, panic attacks, obsessive-compulsive disorder, or bulimia and phenolphthalein, an ingredient found in over-the-counter laxative products that was withdrawn from the US market due to concerns of carcinogenicity, making it an unapproved drug.
Published
July 13, 2016
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Ultimate Formula Capsules, 250mg, 48-count bottles, Manufactured for: Zi Xiu Tang Success, LLC Trexlertown, PA 18087, USA www.zixiutangsuccess.com

by Bee Extremely Amazed LLC

Reason
Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary supplement. Product found to be tainted with undeclared sibutramine, an appetite suppressant that was withdrawn from the US market for safety reasons, making it an unapproved drug.
Published
July 13, 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.