- Recalling firm
- Ventec Life Systems, Inc.
- Reason for recall
- Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
- Affected products (lot / model / serial)
- All Serial Numbers: UDI: 00855573007822
- Units affected
- 25,112 units
- Distribution pattern
- Distribution US nationwide including Puerto Rico.
- Firm location
- Bothell, WA, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-0133-2027
- Recall initiated
- September 17, 2026
- FDA classification date
- October 20, 2026
- FDA report date
- October 28, 2026
- FDA event ID
- 99835
- Last updated on HTM Vibe
- November 3, 2026
