FDA recall D-0953-2017

Product

QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC 15082-814-79), c) 10mL vial (NDC 15082-814-61), Repackaged by Advanced Pharm, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404.

Reason for recall

Lack of Assurance of Sterility

Distribution

Nationwide with the United States

Key facts

Status

Terminated

Initiation date

2017-06-22

Report date

2017-07-19

Termination date

2017-12-06

Voluntary/Mandated

Voluntary: Firm initiated

Location

Houston, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0953-2017