FDA recall Z-0707-2018

Siemens Medical Solutions USA, Inc · Class II · device

Product

Artis Zee and Zeego, Model Numbers: 10094135, 10094137, 10094141, 10094142, 10094143, 10280959, 10848283 & 10848354

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-0707-2018