FDA recall Z-1000-2023
Siemens Medical Solutions USA, Inc · Class II · device
Product
AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF
Reason for recall
There is potential for the footrest to detach from the patient table during use.
Distribution
Worldwide distribution
Key facts
- Status
- Ongoing
- Initiation date
- 2022-12-09
- Report date
- 2023-01-25
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Malvern, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1000-2023