GE Healthcare recalls Brivo MR355 MRI systems due to potential cryogen ventilation system failures. Affected units may require safety checks to prevent risks.
The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
GE Healthcare is recalling Brivo MR35:5 MRI systems because their cryogen ventilation systems might not meet safety standards. This could lead to safety issues if the system fails during operation.
The cryogen ventilation system might not meet required safety standards, potentially causing issues if the system fails during operation. This could lead to safety hazards in medical environments.
Healthcare facilities using GE Healthcare Brivo MR355 MRI systems are most at risk. Patients and staff could be affected if the system malfunctions.
Check if your MRI system is labeled as GE Healthcare Brivo MR355. The recall applies to all units of this system.
Look for the model number on your MRI system to confirm it's a GE Healthcare Brivo MR355.
The recall states there's a potential risk, but the exact danger level isn't specified in the official notice.
The official notice doesn't provide specific action steps for affected users.
Check the system label for the model number GE Healthcare Brivo MR355.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0611-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0611-2022 from GE Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
