FDA Device recall Z-0787-2022
Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration
- FDA Device
- Class III
- terminated
- Published 2022-03-23
On 2022-03-23 the FDA classified a Class III recall of Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration by Livanova Deutschland, citing one ferrite ring expected to be installed on centrifugal pump system power cable may not be present.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0787-2022 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2021-12-17 |
| Published | 2022-03-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Livanova Deutschland |
| Distribution | FL, NE, TX |
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
One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.
Identifiers
| code_info | CP5 Drive Unit Serial Numbers: 60E03336 60E03339 60E03344 60E03347 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0787-2022%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.