FDA recall Z-0708-2018
Siemens Medical Solutions USA, Inc · Class II · device
Product
Axiom Artis, Model Numbers: 5904433, 5904441, 5904649, 5904656, 5917054, 7007755, 7008605, 7412807, 7413078, 7555357, 7555373, 7727717, 7728350 & 7728392
Reason for recall
Potential for liquid entry
Distribution
U.S. Nationwide
Key facts
- Status
- Terminated
- Initiation date
- 2017-06-06
- Report date
- 2018-03-07
- Termination date
- 2019-05-16
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Malvern, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0708-2018