GE Healthcare Finland Oy recalls

GE Healthcare Finland Oy has 13 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 19 Nov 2025. 13 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is labeling errors.

Total recalls13since 2023

Last 12 months2reported

Class I969% of total

Ongoing13latest 19 Nov 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 2 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 9 69%Class II 4 31%Class III 0 0%

Why ge healthcare finland oy is recalled

Labeling Errors969%
Device Malfunction431%

Product types

Patient Monitors1292%
Hip & Knee Implants18%

By year

2025215%
2024215%
2023969%

Ongoing ge healthcare finland oy recalls

13 active

Reported	Class	Recall	Company	Reason	Where
19 Nov 2025Device	CLASS II	Carescape B450 recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction	Nationwide
19 Nov 2025Device	CLASS II	Battery Flex-3S2P 10.8V 18650 Li-ion Smbus used recalled	GE Healthcare Finland Oy	Device Malfunction	Nationwide
3 Jul 2024Device	CLASS II	Carescape Canvas Smart Display recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction
3 Jul 2024Device	CLASS II	Carescape Canvas Smart Display recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction
12 Jul 2023Device	CLASS I	TruSignal Ear Sensor recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Integrated Ear Sensor with GE Connector recalled	GE Healthcare Finland Oy	Labeling Errors	N/A

All ge healthcare finland oy recalls, newest first

13 total

Reported	Class	Recall	Company	Reason	Where
19 Nov 2025Device	CLASS II	Carescape B450 recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction	Nationwide
19 Nov 2025Device	CLASS II	Battery Flex-3S2P 10.8V 18650 Li-ion Smbus used recalled	GE Healthcare Finland Oy	Device Malfunction	Nationwide
3 Jul 2024Device	CLASS II	Carescape Canvas Smart Display recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction
3 Jul 2024Device	CLASS II	Carescape Canvas Smart Display recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Device Malfunction
12 Jul 2023Device	CLASS I	TruSignal Ear Sensor recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Integrated Ear Sensor with GE Connector recalled	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Integrated Ear Sensor with Datex Connector recalled	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Wrap Sensor recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Adult/Pediatric Sensor recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Integrated Ear Sensor with Datex Connector recalled	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Integrated Ear Sensor with Ohmeda Connector recalled	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal AllFit Sensor: a) recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A
12 Jul 2023Device	CLASS I	TruSignal Sensitive Skin Sensor recalled by GE Healthcare Finland Oy	GE Healthcare Finland Oy	Labeling Errors	N/A

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.