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 B…

Recall date

December 31, 2015

Source

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

Recall number

D-0778-2016

FDA classification

Class III

Brand / firm

Pharmedium Services, LLC

Sold / distributed

Nationwide

Why it was recalled

Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration

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

What was recalled

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