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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 11,361–11,380 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL), Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-001-04

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Lidocaine HCl 1%, 10 mL Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-002-03

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL Single-Dose Syringe, For IV Use, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-028-15

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride, 100 mL* Bag, Epidural Use Only, Single-Dose Bag, Hospital/Office Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-080-75

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-61

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37

by Cantrell Drug Company

Reason
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Recall initiated
November 18, 2016
Reported by FDA
December 21, 2016
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

USCG Boat Response Kit - Product Code 80-0353, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Recall initiated
September 27, 2016
Reported by FDA
December 14, 2016
Distribution
Nationwide, Australia & Switzerland

View recall →

Drug Recall Terminated Historical recordClass II

Aid Backpack Kit - Product Code 85-0917, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Recall initiated
September 27, 2016
Reported by FDA
December 14, 2016
Distribution
Nationwide, Australia & Switzerland

View recall →

Drug Recall Terminated Historical recordClass II

Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Recall initiated
September 27, 2016
Reported by FDA
December 14, 2016
Distribution
Nationwide, Australia & Switzerland

View recall →

Drug Recall Terminated Historical recordClass II

Amphibious Trauma Kit - Product Code 85-0639, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Recall initiated
September 27, 2016
Reported by FDA
December 14, 2016
Distribution
Nationwide, Australia & Switzerland

View recall →

Drug Recall Terminated Historical recordClass II

K-9 Trauma Field Kit - Product Code 80-0211, 80-0304, 80-0209, 80-0210, 80-0300, 80-0301, North American Rescue

by North American Rescue LLC.

Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Recall initiated
September 27, 2016
Reported by FDA
December 14, 2016
Distribution
Nationwide, Australia & Switzerland

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.