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…

Recall date

December 16, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0626-2020

FDA classification

Class III

Brand / firm

Pharmedium Services, LLC

Sold / distributed

Nationwide in the U.S.

Why it was recalled

Subpotent Drug

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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.