US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 21, 2019 (7 years ago)

PF-Succinylcholine Chloride Injection

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

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.

Recalling firm
Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
NDC code
69374-919-10
Origin
SC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0154-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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