Magnetom Aera & Skyra (2020-04-16)

Recall Summary Siemens Healthineers has recalled certain Magnetom Aera and Skyra MRI machines distributed across Canada due to a medical device issue. The recall is classified as Class I, indicating a serious safety concern. The specific technical details of the defect and affected serial numbers are not provided in this summary.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-05-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8f7c0b3e-b166-4736-9837-65b633090a8d