-series (a5/a7) Anesthesia Delivery System

Recall Summary Philips is recalling certain A-Series anesthesia delivery systems (models A5 and A7) distributed across Canada due to a potential malfunction that could affect the delivery of anesthesia during surgery. The systems may fail to deliver the correct concentration of anesthetic gases to patients. This recall affects healthcare facilities and hospitals that use these anesthesia machines.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c1647472-0a39-4dbf-8de7-f9b75680867b