Sarns Modular Perfusion System 8

SARNS Modular Perfusion System 8000 Recall The SARNS Modular Perfusion System 8000, a medical device used for blood circulation support during heart surgery, is being recalled across Canada due to potential malfunctions in its control systems that could affect patient safety. The device may not operate as intended during critical procedures. This recall affects hospitals and surgical centers that use this equipment.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-31

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4f69e8cc-8046-4f90-a2be-86f9567646f2