GE Healthcare recalls Revolution CT systems due to potential scan group name input errors causing failed image acquisition. Affected units may not confirm group addition to scans, risking incomplete imaging. Contact GE for remedy details.
When adding one or more intended scan groups names must contain only letters, numbers (0-9), or a space or the user interface will not update to confirm the intended group(s) has been added to the acquisition.
GE Healthcare is recalling Revolution CT scanners because users might enter scan group names with invalid characters, causing the system to fail confirming the group is added to scans. This could lead to incomplete imaging during medical procedures.
The system requires scan group names to contain only letters, numbers, or spaces. If invalid characters are used, the system won't confirm the group is added to scans, potentially causing incomplete imaging during medical procedures.
Medical professionals using GE Healthcare Revolution CT scanners for medical imaging. Patients undergoing CT scans with these systems may be affected if the scan group names are entered incorrectly.
Revolution CT scanners from GE Healthcare. The specific model is not listed in the recall notice, but the system is used for CT imaging of organs like the brain, heart, and liver.
Verify scan group names contain only letters, numbers, or spaces to ensure proper system updates.
The system may not confirm scan group addition if names contain invalid characters, potentially causing incomplete imaging.
The recall notice does not specify a remedy; users should check scan group names for valid characters.
GE Healthcare is the manufacturer; contact them directly for assistance with the issue.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2021-2021 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2021-2021 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.
