ProductGuru Recalls

Brand

GE Healthcare Finland Oy: official recall notices

8 official recall or safety notices on this site name GE Healthcare Finland Oy, dated between 2024-04-05 and 2025-09-26. They were issued by 1 authority: US FDA — Medical Devices (8).

Countries where the notices were issued: Finland (8).

Name as written in the notices: GE Healthcare Finland Oy. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

Notices by year

YearNotices
20254
20244

Notices by authority

AuthorityNotices
US FDA — Medical Devices8

All notices

DateAuthorityProductHazard (as classified)
2025-09-26US FDA — Medical DevicesB105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-1—
2025-09-26US FDA — Medical DevicesCARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a—
2025-09-26US FDA — Medical DevicesPortrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms—
2025-09-26US FDA — Medical DevicesBATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Pa—
2024-04-05US FDA — Medical DevicesCARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e—
2024-04-05US FDA — Medical DevicesCARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-01059642, d) 5514418-01—
2024-04-05US FDA — Medical DevicesCARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 20786—
2024-04-05US FDA — Medical DevicesCARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-—

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