FDA-Device2026-10-20Class IPROCESSING DEFECT
Ventec Life Systems V*Home ventilator recalled for potential flow transducer disconnection
What this means
The V*Home ventilator's internal flow transducer cable connector may disconnect from the internal board, causing the device to restart and temporarily stop delivering ventilation therapy. This affects 25,112 units distributed nationwide. No injuries have been reported.
- Check your device serial number against FDA records at fda.gov
- Contact Ventec Life Systems immediately if you own this model
- Do not stop using your ventilator; continue monitoring for unexpected restarts
- Follow any guidance from Ventec or your healthcare provider
The agency's original wording
Hazard
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
Intended for
Adults
Illnesses reported
None reported
Sold states
Distribution US nationwide including Puerto Rico.
Affected count
25,112 units
Manufactured in
22002 26th Ave Se, Bothell, Washington, United States
Products
V*Home, Model Number: PRT-01444-000, Package PN:PRT-01445-000. used for ventilatory support.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0133-2027More Ventec Life Systems recalls
- FDA-Device2026-10-20Ventec Life Systems V+ Pro Emergency ventilator recalled for potential breathing interruption
- FDA-Device2026-10-20Ventec Life Systems VCSN+Pro ventilator recalled for potential loss of ventilation due to connector disconnection
- FDA-Device2026-10-20Ventec Life Systems VC ventilator recalled for internal cable disconnection risk
- FDA-Device2026-10-20Ventec Life Systems VOCSN+Pro ventilator recalled for potential interruption of ventilation therapy
- FDA-Device2026-10-20Ventec Life Systems VOCSN+Pro ventilator recalled for internal connector failure risk
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