LivaNova Deutschland GmbH: Medical Device Recall in 2022 - (Recall #: Z-0787-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class III

Date Initiated: December 17, 2021

Date Posted: March 23, 2022

Recall Number: Z-0787-2022

Event ID: 89312

Reason for Recall:

One ferrite ring expected to be installed on centrifugal pump system power cable may not be present.

Status: Terminated

Product Quantity: 4

Code Information:

CP5 Drive Unit Serial Numbers: 60E03336 60E03339 60E03344 60E03347

Distribution Pattern:

US distribution in states of FL, TX, and NE

Voluntary or Mandated:

Voluntary: Firm initiated