Ventec Life Systems, Inc. recalls V+Pro
- Recalling company
- Ventec Life Systems, Inc.
- Product
- 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.
- Reason
- Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
- Classification
- Class I – a reasonable probability that use will cause serious adverse health consequences or death
- Recall date
- Sep 17, 2026
- Reported
- Oct 28, 2026
- Distribution
- Distribution US nationwide including Puerto Rico.
- Status
- Ongoing
- Quantity
- 39,568 units
- Lot / codes
- All Serial Numbers: PRT-01185-000 -UDI: 00855573007877; PRT-01185-001 - UDI: 00850018761161; PRT-01185-002 - UDI: 00850018761154
- Company location
- Bothell, WA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0129-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0129-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.