Class II — GE Medical Systems Information Technologies Inc
| Recalling firm | GE Medical Systems Information Technologies Inc |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| Product | PORTRAIT CORE SERVICES SOFTWARE V1.1, Ref# 5700209 |
| Quantity | 23 units |
| Distribution | US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom. |
| Initiated | 2026-07-20 |
| Classified | 2026-08-27 |
| Recall number | Z-3036-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — GE Medical Systems Information Technologies Inc (Z-3036-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99536/
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