GE Healthcare recalls CARESCAPE Central Station V2 models 2082278-001 and 2082279-001 due to potential power supply failure causing loss of patient monitoring. Affected units include specific display and component parts.
The CARESAPE Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station.
GE Healthcare is recalling certain CARESCAPE Central Station V2 medical devices because a power supply component failure could shut down the system, leading to loss of patient monitoring. This affects specific model numbers and related display components.
The device can shut down due to a potential failure in the power supply component. This interruption may cause loss of patient monitoring at the central station, which is critical for patient safety during medical procedures.
Healthcare facilities using the CARESCAPE Central Station V2 models 2082278-001 and 2082279-001 are most at risk. Patients in monitored environments could experience loss of critical monitoring if the device shuts down.
Check for model numbers 2082278-001 or 2082279-001 on the device. Affected units also include specific display parts with part numbers starting with 2092930.
Identify the model number on the device label to confirm if it is 2082278-001 or 2082279-001.
Reach out to GE Healthcare for guidance on affected components and next steps.
Models 2082278-001 and 2082279-001, along with specific display and component parts listed in the recall notice.
A potential power supply component failure can cause the device to shut down, leading to loss of patient monitoring.
Check for model numbers 2082278-001 or 2082279-001 on the device label, or specific display parts with part numbers starting with 2092930.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1265-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1265-2022 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.
