Skip to main content
Get Alerts

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.

Filters
Recall details
Location
Date range
Clear filters

Showing 2,701–2,720 of 17,937 drug recalls

Drug Recall Terminated Historical recordClass II

Ceftriaxone for Injection, USP 10 grams per Pharmacy Bulk Package, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-215-15

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

Ceftriaxone for Injection, USP 2 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-214-42

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 250 mg per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017, NDC 66794-211-42

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 1 gram per vial, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-089-02

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

Cefepime for Injection, USP 2 grams per vial, Rx only, Mfg. for: Piramal Critical Care Bethlehem, PA 18017 USA, NDC 66794-210-41

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

Cefepime for Injection, USP 1 gram per vial, Rx only, Mfg. for: Piramal Critical Care Bethlehem, PA 18017 USA, NDC 66794-209-41

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

Cefepime for Injection, USP 2 grams per vial, Rx only, Mfd. for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-009-20

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: Civica Inc. Lehi Utah 84043, NDC 72572-058-10

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 1 gram per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-057-10

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, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-083-01

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

Ampicillin and Sulbactam for Injection, USP 3 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-082-02

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 1.5 grams per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-081-02

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 15 grams per Pharmacy Bulk Package, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-208-15

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 3 grams per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-207-41

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, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-007-75

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 gram per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-022-10

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 gram per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-021-10

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 for Injection, USP 10 grams per Pharmacy Bulk Package, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-088-01

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

Ampicillin for Injection, USP 2 g per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-087-02

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 for Injection, USP 500 mg per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-085-02

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 →

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.