GE Healthcare recalls CARESCAPE ONE patient monitors that may fail to alert for ventricular fibrillation when docked to specific host monitors, posing a risk of undetected cardiac events.
CARESCAPE ONE may not provide visual and audible alarms for Ventricular Fibrillation (V Fib), if V Fib occurs at the time CARESCAPE ONE is docked to a CARESCAPE B450/B650/B850 host monitor.
GE Healthcare is recalling certain CARESCAPE ONE patient monitors that may not provide alarms for ventricular fibrillation (V-Fib) when connected to specific host monitors. This could lead to undetected cardiac events if a patient experiences V-Fib while the monitor is docked.
When the CARESCAPE ONE patient monitor is docked to a compatible host monitor (B450/B650/B850), it may fail to detect and alert for ventricular fibrillation (V-Fib). This could result in undetected cardiac events if a patient experiences V-Fib while the monitor is connected.
Healthcare professionals using the CARESCAPE ONE patient monitor with specific host monitors (B450/B650/B850) in hospitals. Patients at risk during monitoring sessions where the monitor is docked.
Check for the model number 2087075-001 and serial numbers listed in the recall notice. The product is used in hospitals for patient monitoring during transport and in multiple areas.
Ensure the CARESCAPE ONE monitor is not docked to a B450/B650/B850 host monitor when monitoring patients.
The monitor may not provide alarms for ventricular fibrillation (V-Fib) when docked to specific host monitors (B450/B650/B850), which could lead to undetected cardiac events.
Check if your monitor has the model number 2087075-001 and a serial number from the list provided in the recall notice. If it does, ensure it is not docked to a B450/B650/B850 host monitor during use.
The recall notice does not specify a fix or remedy for this 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-2750-2020 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2750-2020 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.
