FDA recall Z-1954-2019

Siemens Medical Solutions USA, Inc · Class II · device

Product

Cios care fusion system

Reason for recall

DAP chamber may be missing an insulating foil

Distribution

IL, NE

Key facts

Status
Terminated
Initiation date
2019-06-20
Report date
2019-07-17
Termination date
2020-04-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1954-2019