FDA recall D-0462-2018

Product

Vecuronium Bromide in Sterile Water for Injection in all strengths, all doses, and all packaging.

Reason for recall

Lack of sterility assurance.

Distribution

U.S.A. Nationwide

Key facts

Status

Terminated

Initiation date

2017-12-27

Report date

2018-02-28

Termination date

2020-05-07

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0462-2018