Official recall record
GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-04-24
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- GE Medical Systems Information Technologies Inc
What the authority reported
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.
Record last checked against the registry on 2026-09-16.
Other recalls from this brand
- 2026-07-20 · US FDA — Medical Devices
PORTRAIT CORE SERVICES SOFTWARE V1.0.5, Ref# 5697353 - 2026-07-20 · US FDA — Medical Devices
PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592 - 2026-07-20 · US FDA — Medical Devices
PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209
All 12 official recall notices naming GE Medical Systems Information Technologies Inc on this site →
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