Chieva 3.0t Mri, Ct, And Xr Systems (2016-10-12)

Recall Summary Philips is recalling ACHIEVA 3.0T MRI, CT, and XR imaging systems distributed across Canada due to a medical device issue. The recall is classified as Class I, indicating a serious safety concern. This recall affects healthcare facilities that use these imaging systems.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-11-03

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ea76d9e7-2dda-4e39-8e98-c9ea47e6ccde