FDA-Device2026-10-20Class IPROCESSING DEFECT
Ventec Life Systems V+ Pro Emergency ventilator recalled for potential breathing interruption
What this means
The V+ Pro Emergency ventilator may experience an internal cable connector disconnection that could cause the device to restart unexpectedly. This restart can interrupt ventilation therapy for patients who depend on the device.
- If you use a Ventec V+ Pro Emergency ventilator (Model PRT-01201-000), contact Ventec Life Systems immediately for instructions.
- Do not stop using your ventilator without medical guidance; speak with your healthcare provider or respiratory therapist right away.
- Have a backup ventilation plan in place while awaiting further guidance from Ventec or your medical team.
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
30,120 units
Manufactured in
22002 26th Ave Se, Bothell, Washington, United States
Products
V+ Pro Emergency, Model Number: PRT-01201-000, Package PN:PRT-01173-000,PRT-01222-000. used for ventilatory support.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0132-2027More Ventec Life Systems recalls
- 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
- FDA-Device2026-10-20Ventec Life Systems VOCSN ventilator recalled for potential ventilation interruption
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