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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.

37,142
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
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
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 13,081–13,100 of 17,335 recalls

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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 →

FDA Recall Terminated Historical recordClass I

SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition

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 →

FDA Recall Terminated Historical recordClass I

SlimeX-15 Capsules, 15 mg, 30-count bottles, Marketed by: Signature Pharmaceuticals Ltd. MUMBAI-400-030 Manufactured in India by: HAB Pharmaceuticals & Research Limited 10-Pharma City, SIDCUL, Selaqui, Dehradun, 248 197

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 →

FDA Recall Terminated Historical recordClass I

Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203

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, 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

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.