FDA recall Z-0683-2024
Siemens Medical Solutions USA, Inc · Class II · device
Product
Sensis Vibe Hemo
Reason for recall
The possibility of the Sensis documentation functionality application to crash.
Distribution
Domestic: CA, CT, & FL.
Key facts
- Status
- Ongoing
- Initiation date
- 2023-11-29
- Report date
- 2024-01-17
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Malvern, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0683-2024