V+Pro Model Number: PRT-01185-000, Package PN:PRT-01198-000; Model Number: PRT-01185-001, Package PN: N/A; Model Number: PRT-01185-002, Package PN:N/A. used for ventilatory support.

Class I

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: PRT-01185-000 -UDI: 00855573007877; PRT-01185-001 - UDI: 00850018761161; PRT-01185-002 - UDI: 00850018761154
Units affected: 39,568 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-0129-2027
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