September 10, 2019

FDA: Hospira recalls one lot of Bacteriostatic Water for Injection

By: Judy Mathias

Editor's Note

The Food & Drug Administration on September 6 posted Hospira, Inc’s recall of one lot of Bacteriostatic Water for Injection, USP, 30 mL, multi-dose vials, lot W20308.

The recall was initiated because of the potential for a lack of sterility assurance.

Sponsored Message

To date, Hospira has not received any reports of adverse events associated with this issue for this lot.


Sign Up For OR a.m.
Sign up for the free OR a.m. eLetter to get news like this in your inbox every morning!

OR Manager Jobs
Live chat by BoldChat