Siemens Medical Solutions USA, Inc Recall 93637
Description: Sensis Vibe Hemo
Siemens Medical Solutions USA, Inc Recall 93637 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-0683-2024 |
| Event ID | 93637 |
| Event Description | Sensis Vibe Hemo |
| Product Type | Devices |
| Distribution | Domestic: CA, CT, & FL. |
| Quantity | 331 units |
| Recall Reason | The possibility of the Sensis documentation functionality application to crash. |
| Device Classification | 20240117 |
| Device Code Info | Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015. |
| Center Classification Date | 20240109 |
| Recall Initiation Date | 20231129 |
| Recalling Firm | Siemens Medical Solutions USA, Inc |
| Initial Notification | Letter |
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