Sorin Centrifugal Pump System — Class III medical device recall Z-0787-2022
Terminated recall by LivaNova Deutschland GmbH, reported 2022-03-23, distributed in FL, NE, TX. One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.
| Recall number | Z-0787-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LivaNova Deutschland GmbH, Munich, N/A, Germany |
| Recall initiated | 2021-12-17 |
| Classified | 2022-03-15 |
| Reported by FDA | 2022-03-23 |
| Terminated | 2024-01-08 |
| Distributed | FL, NE, TX |
| Quantity | 4 |
| UPC / GTIN / UDI-DI | 04033817900948 |
| Serial numbers | 60E03336, 60E03339, 60E03344, 60E03347 |
| Model numbers | 60-01-04 |
Product
Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration. A cardiopulmonary bypass speed control device.
Reason for recall
One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.
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-0787-2022. 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.