Pharmedium Services, LLC recalls NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex
Recalled January 1, 2020 · FDA recall D-0626-2020 · Pharmedium Services
Hazard
Subpotent Drug · FDA Class III
Units
864 bags
Sold at
Nationwide in the U.S.
Description
Subpotent Drug
Product
NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Injection USP (16 mcg per mL) Total Volume 508.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
Manufacturer(s)
Pharmedium Services, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →