Drug Recall
Terminated
Historical recordClass II
Ketamine HCl Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Ephedrine Sulfate Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Fentanyl Citrate Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Midazolam HCl Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Methadone HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Labetalol HCl in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Potassium Chloride in 5% Dextrose in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Phenylephrine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Dexamethasone Sodium Phosphate in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Adenosine Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Succinylcholine Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Potassium Chloride in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Fentanyl Citrate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Lidocaine HCl in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Morphine Sulfate in 5% Dextrose in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Morphine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Midazolam HCl in 5% Dextrose in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
Midazolam HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
Drug Recall
Terminated
Historical recordClass II
HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
by PharMEDium Services, LLC
- Reason
- Lack of sterility assurance.
- Recall initiated
- December 27, 2017
- Reported by FDA
- February 28, 2018
- Distribution
- U.S.A. Nationwide
View recall →
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.