FDA recall D-0626-2020

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.

Reason for recall

Subpotent Drug

Distribution

Nationwide in the U.S.

Key facts

Status

Terminated

Initiation date

2019-12-16

Report date

2020-01-01

Termination date

2021-02-09

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0626-2020