GE Healthcare recalls CT Goldseal BrightSpeed 16 PWR TIO 2 YR systems with improper electrical wiring to UPS. Affected units may have safety risks during power outages.
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 CT scanners that may not be properly wired to the power supply system. This could cause safety issues during power outages if the system loses power unexpectedly.
The CT systems may not be wired correctly to the Uninterruptible Power Supply (UPS). This means that during power outages, the system could lose power unexpectedly, potentially causing safety risks for patients and staff.
Medical facilities that installed GE CT Goldseal BrightSpeed 16 PWR TIO 2 YR systems with GE supplied A! electrical panels. Patients and staff at these facilities are at risk during power outages.
Check for the model name 'CT Goldseal BrightSpeed 16 PWR TIO 2 YR' and serial number 194800HM9 or System ID Number ALLIANCECT171. The recall applies to systems installed with GE supplied A! electrical panels.
Verify if the CT system was installed with a GE supplied A! electrical panel.
Some CT and CT/PET systems installed with GE supplied A! electrical panels may not be properly wired to the partial system UPS, which could cause safety risks during power outages.
Check for the model name 'CT Goldseal BrightSpeed 16 PWR TIO 2 YR' and serial number 194800HM9 or System ID Number ALLIANCECT171. The recall applies to systems installed with GE supplied A! electrical panels.
The recall requires checking if your system was installed with a GE supplied A! electrical panel. If affected, contact GE Healthcare for further instructions.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2587-2018 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2587-2018 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.
