Drug recall

PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL…

FDA recall event 84106 · Class III · Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Key facts

Event ID 84106
Recall numbers D-0154-2020
Recalling firm Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
Product type Drugs
Products 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…
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Incorrect labeling: Incorrect or missing lot and/or exp date
Initiation date Oct 21, 2019
Report date Nov 6, 2019
Termination date May 7, 2020
City West Columbia
State SC
Country United States
FEI number 3011158388

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

Browse all FDA drug and product recalls