Medical Device Recall: PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209
GE Medical Systems Information Technologies Inc · July 20, 2026
Reason for Recall
Software 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.
Distribution
US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom.
States Affected
MI, NY
Quantity Affected
23 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3036-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.