FDA recall Z-0706-2018
Siemens Medical Solutions USA, Inc · Class II · device
Product
Artis Q and Q.Zen, Model Numbers:10848280, 10848281, 10848282, 10848353 & 10848355
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-0706-2018