Magnetom Prisma And Prisma Fit (2018-12-11)

MAGNETOM Prisma and Prisma Fit Recall Summary Siemens is recalling MAGNETOM Prisma and Prisma Fit MRI machines distributed across Canada due to a software issue that could cause the devices to malfunction during operation. The recall affects hospitals and medical facilities that use these 2018 or earlier models. This is a Class I recall, meaning the defect poses a serious risk to patient safety.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-01-08
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/55bd7580-6b66-49d8-bbbd-e95a0ea86028