GE Medical Systems Information Technologies recalls

GE Medical Systems Information Technologies has 19 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 23 Sep 2026. 18 are still ongoing. 14 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls19since 2017
Last 12 months14reported
Class I00% of total
Ongoing18latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 19 100%Class III 0 0%

Why ge medical systems information technologies is recalled

By year

Ongoing ge medical systems information technologies recalls

18 active

All ge medical systems information technologies recalls, newest first

19 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IICarescape Central Station CSCS V3 MAS800 Desktop recalledGE Medical Systems Information TechnologiesDevice MalfunctionNationwide
DeviceCLASS IIPortrait Core Services recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionMI, NY
DeviceCLASS IIFru (Field replaceable unit), Portrait Core Services SW Reload V1.1 recalledGE Medical Systems Information TechnologiesDevice MalfunctionMI, NY
DeviceCLASS IIPortrait Compute And Core Services V1.2 recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionMI, NY
DeviceCLASS IIPortrait Core Services recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionMI, NY
DeviceCLASS IIGE Healthcare Portrait Core Services SW recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionNationwide
DeviceCLASS IIGE Healthcare MAC VU360 recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionNationwide
DeviceCLASS IICASE v7.0 Cardiac Testing System recalled by GE Medical SystemsGE Medical Systems Information TechnologiesOtherNationwide
DeviceCLASS IIGE HealthCare Carescape Telemetry Server V5 Ato recalledGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIGE HealthCare Apexpro v5.0 - ARK2250 recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIGE HealthCare Iou Assy ARK2250 Carescape Telemetry Server recalledGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIGE HealthCare Carescape Telemetry Server Ark- - North America recalledGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIGE HealthCare ApexPro v6.0 eDelivery recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIGE HealthCare Trade IN Carescape Telemetry Server Ark recalledGE Medical Systems Information TechnologiesDevice MalfunctionWI
DeviceCLASS IIMUSE 5 Systems recalled by GE Medical SystemsGE Medical Systems Information TechnologiesOtherNationwide
DeviceCLASS IIPrucka 3 Amplifier recalled by GE Medical SystemsGE Medical Systems Information TechnologiesOtherNationwide
DeviceCLASS IIGE HealthCare Critikon One-cuf blood pressure cuffs recalledGE Medical Systems Information TechnologiesLabeling ErrorsNationwide
DeviceCLASS IIPrucka 3 Amplifiers recalled by GE Medical SystemsGE Medical Systems Information TechnologiesTemperature Abuse17 states
DeviceCLASS IICarescape Patient Data Module (PDM) v2.6 recalled by GE Medical SystemsGE Medical Systems Information TechnologiesDevice MalfunctionNY, WI

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.