Dvanced Perfusion System 1 (2015-05-08)

Recall Summary Abbott Diagnostics is recalling Advanced Perfusion System 1 devices distributed across Canada because they may deliver inaccurate test results due to a software defect. The devices are used to measure organ perfusion during medical procedures. Healthcare facilities that received these devices are affected by this recall.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2015-06-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/383f01bb-1780-44e3-ac7e-69c8c8adf324