Pharmedium Services, LLC recalls NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Bl
Recalled March 23, 2016 · FDA recall D-0778-2016 · Pharmedium Services
Hazard
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration · FDA Class III
Sold at
Nationwide
Description
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Product
NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
Manufacturer(s)
Pharmedium Services, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →