Reported Nov 19, 2025 · Ongoing
CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a…
GE Healthcare Finland Oy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE Healthcare Finland Oy · Kuortaneenkatu 2 · Helsinki · N/A
Is this the product you have?
- CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
- Lot codes and dates
- UDI-DI 00195278288639 Serial numbers
2,326 of 2,326 codes
SV925270018SASV925270014SASV925270015SASV925260105SASV925270020SASV925270013SASV925270017SASV925270016SASV925060394SASV925080329SASV925080345SASV925080323SASV925080348SASV925080153SASV925080340SASV925080281SASV925080346SASV925290119SASV925290090SASV925180134SASV925160111SASV925180131SASV925180139SASV925180140SASV925180142SASV925180143SASV925180151SASV925180152SASV925160114SASV925180141SASV925180126SASV925180132SASV925180136SASV925180135SASV925180144SASV925180146SASV925180149SASV925270007SASV925260094SASV925270009SASV925270010SASV925270008SASV925260111SASV925270003SASV925270011SASV925260085SASV925260113SASV925270001SASV925270002SASV925270006SASV925270012SASV925270005SASV925270004SASV925190002SASV925180193SASV925100151SASV925100149SASNA24400063SASV925190009SASV925200017SA
- UDI-DI 00195278288639 Serial numbers
- Amount recalled
- 5935
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new GE Healthcare Finland Oy recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.