- Recalling firm
- GE Medical Systems Information Technologies Inc
- 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.
- Affected products (lot / model / serial)
- UDI-DI (GTIN) 00195278679307
- Units affected
- 0
- Distribution pattern
- US: MI, NY and Australia, Czech Republic, Finland, Germany, Italy, Netherlands, Qatar, Saudi Arabia, Switzerland, United Arab Emirates, United Kingdom.
- Firm location
- Waukesha, WI, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3039-2026
- Recall initiated
- July 20, 2026
- FDA classification date
- August 27, 2026
- FDA report date
- September 2, 2026
- FDA event ID
- 99536
- Last updated on HTM Vibe
- September 8, 2026