FDA recall record

LivaNova Deutschland GmbH Sorin Centrifugal Pump System, CP5, Drive Unit recall — FDA Z-0787-2022

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

Class IIIclassification
Z-0787-2022official record ID
Mar 23, 2022report date

Recall record at a glance

Official recordZ-0787-2022
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLivaNova Deutschland GmbH
Report dateMar 23, 2022
Recall initiation dateDec 17, 2021
Quantity4
LocationMunich, N/A, Germany

Official 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.

Why the product was recalled

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

Distribution information

US distribution in states of FL, TX, and NE

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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