Ge Healthcare Finland Oy recalls
Ge Healthcare Finland Oy appears in 22 official U.S. recall notices indexed by RecallRadar, most recently on 2025-11-19.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
FDA Device · Class II · 2025-11-19 · Ge Healthcare Finland Oy - CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor,…
FDA Device · Class II · 2025-11-19 · Ge Healthcare Finland Oy - BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, r…
FDA Device · Class II · 2025-11-19 · Ge Healthcare Finland Oy - B105P, B125P, B105M, B125M, B155M Patient Monitors
FDA Device · Class II · 2025-11-19 · Ge Healthcare Finland Oy - Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Ph…
FDA Device · Class II · 2025-11-19 · Ge Healthcare Finland Oy - CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-01023150, 4) 2095801-001-0…
FDA Device · Class II · 2024-07-03 · Ge Healthcare Finland Oy - CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102
FDA Device · Class II · 2024-07-03 · Ge Healthcare Finland Oy - CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 2078633-017, 5) 2078633-028, 6)…
FDA Device · Class II · 2024-07-03 · Ge Healthcare Finland Oy - CARESCAPE Canvas 1000, Model Numbers: a) 5865770
FDA Device · Class II · 2024-07-03 · Ge Healthcare Finland Oy - CARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-01059642, d) 5514418-01080402, e) 5514418-0108131…
FDA Device · Class II · 2024-07-03 · Ge Healthcare Finland Oy - TruSignal Sensitive Skin Sensor, REF TS-SE-3
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-GE
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Wrap Sensor, REF TS-W-D
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Integrated Ear Sensor with Ohmeda Connector REF TS-E4-H
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Ear Sensor, REF TS-E-D
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - TruSignal Adult/Pediatric Sensor
FDA Device · Class I · 2023-07-12 · Ge Healthcare Finland Oy - GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of CARESCAPE B850 V2 in 510(k) countries [UR_CRSCP-1046]: The CARESCAPE M…
FDA Device · Class II · 2018-10-17 · Ge Healthcare Finland Oy - GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of CARESCAPE B450 in 510(k) countries [UR_CRSCP-885]: The CARESCAPE Monit…
FDA Device · Class II · 2018-10-17 · Ge Healthcare Finland Oy - GE Healthcare CARESCAPE Monitor B650
FDA Device · Class II · 2018-07-11 · Ge Healthcare Finland Oy