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Hospira Issues a Voluntary Recall for Certain Naloxone Lot Numbers

Hospira, Inc., a Pfizer company, is voluntarily recalling lots 72680LL and 76510LL of Naloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL, Carpuject Single-use cartridge syringe system (NDC 0409-1782-69), to the hospital/institution level due to the potential presence of embedded and loose particulate matter on the syringe plunger. These Lot numbers have already been found in WVEMS Drug Boxes in the Region. 

Click here for the FDA Recall

 

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