FDA Device recall Z-0683-2024
Sensis Vibe Hemo
- FDA Device
- Class II
- ongoing
- Published 2024-01-17
On 2024-01-17 the FDA classified a Class II recall of Sensis Vibe Hemo by Siemens Medical Solutions Usa, citing the possibility of the Sensis documentation functionality application to crash.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0683-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-29 |
| Published | 2024-01-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | CA, CT, FL |
Product
Sensis Vibe Hemo
Reason
The possibility of the Sensis documentation functionality application to crash.
Identifiers
| code_info | Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0683-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.