September 10, 2019
FDA: Hospira recalls one lot of Bacteriostatic Water for Injection
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.
To date, Hospira has not received any reports of adverse events associated with this issue for this lot.
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