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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 2,841–2,860 of 18,047 drug recalls

Drug Recall Ongoing Historical recordClass II

VANComycin 1.5g added to 250 mL of 0.9% Sodium Chloride Injection, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-184-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

FentaNYL 500 mcg (2mcg/mL) and Ropivacaine HCL 250 mg (0.1%) added to 250 mL 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-950-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

VANComycin 750mg added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-255-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

Norepinephrine 4 mg added to 250 mL of 5% Dextrose Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-500-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

VANComycin 1.25g added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-264-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

VANComycin 1.25g added to 250 mL of 0.9% Sodium Chloride Injection, Rx Only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-284-25

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Ongoing Historical recordClass II

Ketamine Injection, 50 mg per 5 mL (10 mg/mL), Single-Use Syringe, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-050-05

by Apollo Care, LLC

Reason
Lack of Assurance of Sterility
Recall initiated
May 2, 2023
Reported by FDA
May 24, 2023
Distribution
Missouri only

View recall →

Drug Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 4.5 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-080-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP 2.25 g per vial,s Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-078-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 3.375 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-217-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP, 2.25 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC66794-216-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Piperacillin and Tazobactam for Injection, USP 4.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-004-51

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ceftriaxone for Injection, USP 10 grams per Pharmacy Bulk Package, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-098-01

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ceftriaxone for Injection, USP 1 gram per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-213-42

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ceftriaxone for Injection, USP 500 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-212-42

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Cefepime for Injection, USP 2 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-090-02

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 3 grams vials, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-242-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 15 grams per Pharmacy Bulk Package, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-243-15

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-241-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-206-41

by Astral SteriTech Private Ltd.

Reason
Lack of Assurance of Sterility
Recall initiated
May 15, 2023
Reported by FDA
May 24, 2023
Distribution
Nationwide within the United States

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.

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