FDA recall Z-1001-2023
Siemens Medical Solutions USA, Inc · Class II · device
Product
AXIOM Luminos Agile
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-1001-2023