GE Healthcare recalls various MRI systems with specific software versions that may have incorrect software loaded. Affected models include Signa 1.0T Horizon, Profile, and others. No immediate action is required but users should check their software version.
Possible incorrect software version loaded.
GE Healthcare is recalling various MRI systems that may have an incorrect software version loaded. This could potentially cause imaging errors but does not pose an immediate risk to safety. Affected models include Signa 1.0T Horizon, Profile, and others. Users should check their software version and contact GE Healthcare if needed.
The software version may be incorrect, which could lead to imaging errors or inaccurate results. However, this does not involve physical harm or safety risks in normal use.
Medical facilities and MRI system users who own or operate the affected GE Healthcare MRI systems. Most at risk are healthcare providers using the specific models listed in the recall.
Check your MRI system's model and software version. Affected models include Signa 1.0T Horizon 5.X HISPE, Profile, and others listed in the recall. The software version may be incorrect.
Identify your MRI system model and software version to see if it matches the affected models listed in the recall.
No, this recall is for potential imaging errors due to incorrect software, not a safety hazard. The risk is low and does not involve physical harm.
No, you do not need to stop using your system. The recall does not require immediate action but checking the software version is recommended.
Check your MRI system's model and software version against the list of affected models provided in the recall notice.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0693-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0693-2019 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.
