ClearanceBrief
Recall Z-3037-2026 · MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

GE Medical Systems Information Technologies Inc

PORTRAIT COMPUTE AND CORE SERVICES V1.2, Ref# 5700592

DateAug 27, 2026 (initiated Jul 20, 2026)
StatusOpen, Classified
ReasonSoftware issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured for each patient or care area.
Root causeDevice Design
ActionGE Healthcare issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 7/20/2026 by letter delivered using traceable means. The notice explained the issue, potential risk, and requested the following: "Actions to be taken by Customer/User You can continue to use your Portrait Mobile Monitoring Solution with Portrait Core Services SW V1.0.5, V1.1 or V1.2. Please ensure appropriate alternative monitoring is established for patients before a software update is started. A User Manual addendum is included with this letter that includes specific instructions related to alterna
Quantity4 units
DistributionUS: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K234130Portrait™ Mobile Monitoring Solution consists of: • Portrait™ Central Viewer Application (Portrait CVAXB) • Portrait™
Ge Medical Systems Information Technologies, Inc., Mar 20, 2024