PF-Succinylcholine Chloride Injection recalled over labeling errors

Recall date

October 21, 2019

Source

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

Official notice title

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center recalls PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-fi…

Recall number

D-0154-2020

FDA classification

Class III

Brand / firm

Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Sold / distributed

Nationwide in the U.S.

Why it was recalled

Incorrect labeling: Incorrect or missing lot and/or exp date

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

What was recalled

PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B Outsourcing Facility 4500 12th St. Ext West Columbia, SC 29172, NDC 69374-919-10.