PlainRecalls
FDA Drug Moderate Class II Terminated

Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for: AuroMedics Pharma, LLC, NDC 55150-243-46.

Reported: May 9, 2018 Initiated: March 27, 2018 #D-0704-2018

Product Description

Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for: AuroMedics Pharma, LLC, NDC 55150-243-46.

Reason for Recall

Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap

Details

Recalling Firm
AuroMedics Pharma LLC
Units Affected
46824 bags
Distribution
US Nationwide
Location
East Windsor, NJ

Frequently Asked Questions

What product was recalled?
Levofloxacin in 5% Dextrose Injection, 250 mg Levofloxacin (5 mg/mL) in 50 mL of 5% Dextrose, For Intravenous Infusion, Rx only, Manufactured By: Aurobindo Pharma Limited IDA Pashamylaram - 502307, India, Manufactured for: AuroMedics Pharma, LLC, NDC 55150-243-46.. Recalled by AuroMedics Pharma LLC. Units affected: 46824 bags.
Why was this product recalled?
Lack of Assurance of Sterility; confirmed customer report of a leaking bags and mold found between the outer bag and the overwrap
Which agency issued this recall?
This recall was issued by the FDA Drug on May 9, 2018. Severity: Moderate. Recall number: D-0704-2018.