--- title: "GE Healthcare Finland Oy Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search GE Healthcare Finland Oy recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/ge-healthcare-finland-oy/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # GE Healthcare Finland Oy recall records **19** reported ongoing 19 records in this archive. Latest source date Sep 26, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Sep 26, 2025 FDA device enforcement ### [Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia ...](https://isitonrecall.com/recall/fda-device-z-0453-2026-carescape-b450-model-no-5805686-shipped-with-potentially-affected-batteries-or-affected-batteries-in/) 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 re... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batte...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0453-2026%22) Sep 26, 2025 FDA device enforcement ### [CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythm...](https://isitonrecall.com/recall/fda-device-z-0454-2026-carescape-one-model-no-2087075-300-shipped-with-potentially-affected-batteries-or-affected-batteries/) 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 re... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected ba...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0454-2026%22) Sep 26, 2025 FDA device enforcement ### [B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 616000...](https://isitonrecall.com/recall/fda-device-z-0455-2026-b105p-b125p-b105m-b125m-b155m-patient-monitors-model-nos-6160000-002-6160000-003-6160000-004-6160000/) 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 re... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-00...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0455-2026%22) Sep 26, 2025 FDA device enforcement ### [Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms](https://isitonrecall.com/recall/fda-device-z-0456-2026-portrait-vsm-model-nos-6660000-666-monitor-physiological-patient-with-arrhythmia-detection-or-alarms/) 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 re... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0456-2026%22) Sep 26, 2025 FDA device enforcement ### [BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S](https://isitonrecall.com/recall/fda-device-z-0457-2026-battery-flex-3s2p-10-8v-18650-li-ion-smbus-used-with-affected-patient-monitors-model-no-2062895-001/) 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 re... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution. [Official source for BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-0...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0457-2026%22) Apr 5, 2024 FDA device enforcement ### [CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e) 5865770-01054698; f) 5865770-01054721; g) 5865770-01054740; h...](https://isitonrecall.com/recall/fda-device-z-2168-2024-carescape-canvas-1000-model-numbers-a-5865770-b-5865770-01040169-c-5865770-01054142-d-5865770-010546/) 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 replacement of the CPU timekeeper battery, ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 58...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2168-2024%22) Apr 5, 2024 FDA device enforcement ### [CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monitor, physiological, patient](https://isitonrecall.com/recall/fda-device-z-2169-2024-carescape-canvas-smart-display-model-numbers-a-5700023-b-5700023-02-c-5939590-102-monitor-physiologi/) 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 replacement of the CPU timekeeper battery, ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for CARESCAPE Canvas Smart Display, Model Numbers: a) 5700023, b) 5700023-02, c) 5939590-102; monitor...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2169-2024%22) Apr 5, 2024 FDA device enforcement ### [CARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-01059642, d) 5514418-01080402, e) 5514418-01081317, f) 5514418-01086007, g) 5514418-010...](https://isitonrecall.com/recall/fda-device-z-2170-2024-carescape-canvas-smart-display-model-numbers-a-5514418-b-5514418-maep2-c-5514418-01059642-d-5514418/) 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 replacement of the CPU timekeeper battery, ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for CARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-0105964...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2170-2024%22) Apr 5, 2024 FDA device enforcement ### [CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-01023150, 4) 2095801-001-01023151, 5) 2095801-001-01023152, 6) 2...](https://isitonrecall.com/recall/fda-device-z-2171-2024-carescape-b650-model-numbers-a-mbb313-model-numbers-1-2095801-001-2-2095801-001-01018416-3-2095801-0/) 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 replacement of the CPU timekeeper battery, ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416,...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2171-2024%22) Apr 5, 2024 FDA device enforcement ### [CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 2078633-017, 5) 2078633-028, 6) 2095802-001-54069330, 7) 2095802-001-5...](https://isitonrecall.com/recall/fda-device-z-2172-2024-carescape-b850-model-numbers-a-mbc303-model-numbers-1-2078633-001-2-2078633-010-3-2078633-012-4-2078/) 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 replacement of the CPU timekeeper battery, ... Class II Reported ongoing Distribution: Worldwide distribution. [Official source for CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 207863...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2172-2024%22) May 19, 2023 FDA device enforcement ### [TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs](https://isitonrecall.com/recall/fda-device-z-2026-2023-trusignal-adult-pediatric-sensor-oximeter-ear-a-ref-ts-ap-10-10-pcs-b-ref-ts-ap-25-25-pcs/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Adult/Pediatric Sensor; Oximeter, Ear: a) REF TS-AP-10, 10 pcs; b) REF TS-AP-25, 25 pcs](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2026-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs; B) REF AF-25, 25 pcs; Oximeter](https://isitonrecall.com/recall/fda-device-z-2027-2023-trusignal-allfit-sensor-a-ref-ts-af-10-10-pcs-b-ref-af-25-25-pcs-oximeter/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal AllFit Sensor: a) REF TS-AF-10, 10 pcs; B) REF AF-25, 25 pcs; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2027-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter](https://isitonrecall.com/recall/fda-device-z-2028-2023-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. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Sensitive Skin Sensor, REF TS-SE-3; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2028-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Wrap Sensor, REF TS-W-D; Oximeter](https://isitonrecall.com/recall/fda-device-z-2029-2023-trusignal-wrap-sensor-ref-ts-w-d-oximeter/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Wrap Sensor, REF TS-W-D; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2029-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Ear Sensor, REF TS-E-D; Oximeter](https://isitonrecall.com/recall/fda-device-z-2030-2023-trusignal-ear-sensor-ref-ts-e-d-oximeter/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Ear Sensor, REF TS-E-D; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2030-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE; Oximeter, Ear](https://isitonrecall.com/recall/fda-device-z-2031-2023-trusignal-integrated-ear-sensor-with-ge-connector-ref-ts-e2-ge-oximeter-ear/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Integrated Ear Sensor with GE Connector REF TS-E2-GE; Oximeter, Ear](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2031-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-GE; Monitor, physiological, patient(with arrhythmia detection or alarms)](https://isitonrecall.com/recall/fda-device-z-2032-2023-trusignal-integrated-ear-sensor-with-datex-connector-ref-ts-e4-ge-monitor-physiological-patient-with/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-GE; Monitor, physiological, patie...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2032-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter](https://isitonrecall.com/recall/fda-device-z-2033-2023-trusignal-integrated-ear-sensor-with-datex-connector-ref-ts-e4-n-oximeter/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Integrated Ear Sensor with Datex Connector, REF TS-E4-N; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2033-2023%22) May 19, 2023 FDA device enforcement ### [TruSignal Integrated Ear Sensor with Ohmeda Connector REF TS-E4-H; Oximeter](https://isitonrecall.com/recall/fda-device-z-2034-2023-trusignal-integrated-ear-sensor-with-ohmeda-connector-ref-ts-e4-h-oximeter/) There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. Class I Reported ongoing Distribution: Worldwide [Official source for TruSignal Integrated Ear Sensor with Ohmeda Connector REF TS-E4-H; Oximeter](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2034-2023%22) ## Reasons in these listed records - 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 st... - 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 replacement of the CPU timekeeper battery, a mains power loss o... - There is a potential reduction of energy reaching patient during defibrillation, potential contact with unintended voltage, or inaccurate measurement. These examples come from this result page and are not a ranking of every recall reason. ## Checking GE Healthcare Finland Oy ### Is there a recall on ge healthcare finland oy right now? This archive contains 19 records, including 19 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search GE Healthcare Finland Oy](https://isitonrecall.com/check/?q=GE%20Healthcare%20Finland%20Oy) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)