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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 10,481–10,500 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per Carton, 100 vials per case. Hospira, Inc., Lake Forest, IL 60045 USA, NDC: 0409-2634-50

by HOSPIRA INC, LAKE FOREST

Reason
Presence of Particulate Matter: Silicone oil
Recall initiated
July 26, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA. NDC: 0703-0018-01

by HOSPIRA INC, LAKE FOREST

Reason
Presence of Particulate Matter: Silicone oil
Recall initiated
July 26, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Rocuronium Bromide Injection Solution 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-064-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Neostigmine Methylsulfate Injection Solution 5 mL, 5 mg/5 mL (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-046-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Adenosine in 0.9% Sodium Chloride 30mL, 90 mg/30 mL (3 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-236-03

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Phenylephrine HCL in 0.9% Sodium Chloride 10 mL, 1 mg/10 mL (100 mcg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-171-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222; NDC 52533-103-13

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 mL (16 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-134-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 mL (64 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-288-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL (32 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-217-18

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 5 mL, 100 mg/5 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 10 mL, 200 mg/10 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 1 mL 0.2 mg/1 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 2 mL 0.4 mg/2 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-16

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 5 mL 1 mg/5 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-118-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Ephedrine Sulfate Injection Solution 1 mL, 50 mg/1 mL (50 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-258-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 25 mg/5 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

View recall →

Drug Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL, 50 mg/10 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Recall initiated
July 14, 2017
Reported by FDA
August 16, 2017
Distribution
Nationwide within the US

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.