FDA recall D-1526-2019

Geritrex, LLC · Class II · drug

Product

Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16

Reason for recall

cGMP Deviations: Products may have microbial contamination.

Distribution

U.S.A. Nationwide

Key facts

Status
Terminated
Initiation date
2019-05-31
Report date
2019-07-31
Termination date
2024-02-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Middletown, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1526-2019