GE Healthcare Finland Oy recalls
3 official recalls and safety alerts involving GE Healthcare Finland Oy since 2023-07, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with GE Healthcare Finland Oy or the relevant agency.
- 2025-11-19
USGE Healthcare Finland Oy recalls B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102…
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…
- 2024-07-03
- US
GE Healthcare Finland Oy recalls CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e) 5865770-01054698; f)…
GE HealthCare has become aware of the potential for loss of monitoring on CARESCAPE Canvas 1000, CARESCAPE Canvas Smart Display, and certain versions of CARESCAPE B850 and CARESCAPE B650 monitors if, following the…
- 2023-07-12
- US
GE Healthcare Finland Oy recalls TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter
There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement.