Sensis Vibe Hemo — Class II medical device recall Z-0683-2024
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2024-01-17, distributed in CA, CT, FL. The possibility of the Sensis documentation functionality application to crash.
| Recall number | Z-0683-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2023-11-29 |
| Classified | 2024-01-09 |
| Reported by FDA | 2024-01-17 |
| Distributed | CA, CT, FL |
| Quantity | 331 units |
| UPC / GTIN / UDI-DI | 04056869010199 |
| Serial numbers | 106244, 106245, 18009, 18010, 18011, 18014, 18015, 18016, 19001 |
| Model numbers | 11007641 |
Product
Sensis Vibe Hemo
Reason for recall
The possibility of the Sensis documentation functionality application to crash.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0683-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.