FDA recall D-0667-2017

Allergan Sales, LLC · Class III · drug

Product

Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.

Reason for recall

Failed Impurities/Degradation Specifications

Distribution

Nationwide in the US

Key facts

Status
Terminated
Initiation date
2017-03-16
Report date
2017-04-19
Termination date
2019-05-01
Voluntary/Mandated
Voluntary: Firm initiated
Location
Waco, TX, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0667-2017