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GE Medical Systems Information Technologies Inc

GE Medical Systems Information Technologies Inc: 6 recalls listed since May 2026 across FDA.

By year

  • 20266

By agency

  • FDA6

By category

  • Medical Device6

All recalls (6)

Carescape Central Station

Carescape Central Station may not resume patient monitoring for at least 3 minutes after restart, delaying recognition of events.

Moderate risk, FDA, , Device defect

GE Portrait Core Services Software

Software issue may result in a loss of patient monitoring at the Hub and Central Viewer.

Moderate risk, FDA, , Software defect

GE Healthcare Portrait Core Services Software

GE Healthcare Portrait Core Services SW V 1.2.0 patient monitoring system has a software vulnerability that may allow unauthorized access.

Moderate risk, FDA, , Software defect

GE Healthcare MAC VU360 Electrocardiographs

After selecting the order refresh icon, an open preview or review screen might fail to close automatically after 2 minutes of inactivity.

Moderate risk, FDA, , Software defect

CASE v7.0 Cardiac Testing System

The CASE v7.0 Cardiac Testing System can spark at the printer head, potentially causing serious thermal injury.

Moderate risk, FDA, , Device defect

GE HealthCare Carescape Telemetry Server

GE HealthCare CARESCAPE Telemetry Server can have a persistent NO COMM or OFF NETWORK condition, potentially causing loss of ECG and SpO2 monitoring.

Moderate risk, FDA, , Device defect
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