Recall Monitor
Health Products

MAGNETOM Prisma, Vida, Skyra, Verio Systems

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - Radiology
Product: MAGNETOM Prisma, Vida, Skyra, Verio Systems
Issue: Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalogue number
MAGNETOM Prismaserial 16602610849582
MAGNETOM Vidaserial 17721211060815
MAGNETOM Vidaserial 17566411060815
MAGNETOM Vidaserial 17660011060815
MAGNETOM Vidaserial 17651511060815
MAGNETOM Vidaserial 17692311060815
MAGNETOM Vidaserial 17633011060815
MAGNETOM Vidaserial 17732211060815
MAGNETOM Vidaserial 17666211060815
MAGNETOM Vidaserial 17575911060815
MAGNETOM Vidaserial 17660811060815
Tim 4G - Skyra Fitserial 17000610849580
MAGNETOM Verio, Systemserial 4036610276755
MAGNETOM Verio, Systemserial 4047710276755
MAGNETOM Luminaserial 19642711344916
MAGNETOM Luminaserial 19682211344916
Biograph mMR Systemserial 15102210433372
Biograph mMR Systemserial 5106010433372
Biograph mMR Systemserial 15101410433372
Biograph mMR Systemserial 5101810433372
Biograph mMR Systemserial 5106810433372
MAGNETOM Skyraserial 14503410432915
MAGNETOM Skyraserial 4537010432915
MAGNETOM Skyraserial 4624910432915
MAGNETOM Skyraserial 14533510432915
MAGNETOM Skyraserial 4596110432915
MAGNETOM Skyraserial 14524910432915
MAGNETOM Skyraserial 14506910432915
MAGNETOM Skyraserial 4559310432915

Issue

This field safety corrective action addresses a potential safety issue associated with the magnet venting paths of some 3 Tesla MRI systems, which will require on-site inspection. An ice blockage may have built up within the magnet venting system. In the event of a quench, helium gas may be unable to escape through the designed vent paths, leading to a pressure build-up in the helium containment system. This pressure build-up could ultimately rupture the helium containment system, potentially resulting in a helium leak into the scanning room. Recall start date: August 14, 2025

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