FDA recall D-1002-2019

Roberts Home Medical LLC · Class II · drug

Product

Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home Medical, Inc. Germantown, MD. 20875

Reason for recall

CGMP Deviations

Distribution

Product was distributed in MD, VA and the District of Columbia

Key facts

Status
Terminated
Initiation date
2018-12-19
Report date
2019-03-20
Termination date
2019-05-01
Voluntary/Mandated
Voluntary: Firm initiated
Location
Germantown, MD, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1002-2019