FDA recall D-1042-2016

Profarma Distributors LLC · Class II · drug

Product

VERMOX Tablets 500 mg, 1-count box, UPC 501109900596

Reason for recall

CGMP Deviations

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2016-05-11
Report date
2016-06-29
Termination date
2017-01-24
Voluntary/Mandated
Voluntary: Firm initiated
Location
Columbus, OH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1042-2016