GE Healthcare CARESCAPE ONE Patient Monitor May Not Alert for V-Fib During Docking
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.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/64929-ge-healthcare-carescape-one-patient-monitor-may-not-alert-for.
Source Summary by GovInfoNow · govinfonow.com/recall/64929-ge-healthcare-carescape-one-patient-monitor-may-not-alert-for · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2750-2020
Cite this page
“GE Healthcare CARESCAPE ONE Patient Monitor May Not Alert for V-Fib During Docking.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64929-ge-healthcare-carescape-one-patient-monitor-may-not-alert-for. Based on FDA recall #Z-2750-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2750-2020%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
GE Healthcare- Category
Medical device
What to do — step by step
Check Monitor Docking
Ensure the CARESCAPE ONE monitor is not docked to a B450/B650/B850 host monitor when monitoring patients.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 4 states.
FDA distribution: “Worldwide distribution - US Nationwide distribution including in the states of MT, NC, TX and WI. The countries of Australia, Austria, Bahrain,Belgium, Bolivia, Brazil ,Canada, Chile, Check Republic, Denmark, Ecuador, Egypt, Estonia,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Montana, North Carolina, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 4.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2750-2020 (June 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2750-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.