---
title: "Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI... — FDA record Z-0787-2022 | Is It on Recall"
description: "One ferrite ring expected to be installed on centrifugal pump system power cable may not be present."
url: https://isitonrecall.com/recall/fda-device-z-0787-2022-sorin-centrifugal-pump-system-cp5-drive-unit-catalogue-item-60-01-04-udi-04033817900948-used-in-an-h/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 S... — FDA record Z-0787-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 17, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class III
- **Recalling firm**: LivaNova Deutschland GmbH
- **Quantity**: 4
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0787-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0787-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | CP5 Drive Unit Serial Numbers: 60E03336 60E03339 60E03344 60E03347 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution in states of FL, TX, and NE

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Mar 23, 2022
- **Recall initiation date**: Dec 17, 2021
- **Center classification date**: Mar 15, 2022
- **Termination date**: Jan 8, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0787-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [LivaNova Deutschland GmbH records](https://isitonrecall.com/brand/livanova-deutschland-gmbh/)