GE Healthcare recalls Revolution EVO 3.6 CT and CT/PET systems with improper electrical panel wiring to the UPS power supply, potentially causing system failure.
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
GE Healthcare is recalling certain Revolution EVO 3.6 CT and CT/PET systems that may not be properly wired to the UPS power supply. This could lead to system failure during power outages, risking data loss or equipment damage.
The electrical panel may not be correctly connected to the UPS power supply. This could cause the system to fail during power outages, potentially leading to data loss or equipment damage but not immediate injury.
Medical facilities that installed these systems with GE's supplied A! electrical panels. Systems with specific serial numbers and labels (HVY WAUK, LONG HINO, etc.) are affected.
Check for the label on the system: HVY WAUK, LONG HINO, LONG WAUK, MID BJG, or MID WAUK. Look for specific serial numbers listed in the recall notice.
Identify if your system has one of the labels: HVY WAUK, LONG HINO, LONG WAUK, MID BJG, or MID WAUK.
Confirm your system's serial number matches those listed in the recall notice for the specific label.
The electrical panel may not be properly connected to the UPS power supply, which could cause system failure during power outages, potentially leading to data loss or equipment damage.
Check the label on your system (HVY WAUK, LONG HINO, LONG WAUK, MID BJG, or MID WAUK) and verify the serial number against the list provided in the recall notice.
The recall only applies to systems with the specific labels and serial numbers listed. If your system does not match, it is not affected.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2584-2018 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2584-2018 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.
