FDA-Device2026-10-20Class IPROCESSING DEFECT
Ventec Life Systems VC+Pro ventilator recalled for potential loss of ventilation
What this means
The internal flow transducer cable in Ventec's VC+Pro ventilator may disconnect from the circuit board, causing the device to reboot unexpectedly. This interruption could briefly stop ventilation support to the patient.
- If you use or operate a VC+Pro ventilator (Model PRT-00900-100), contact Ventec Life Systems immediately for instructions.
- Do not attempt to repair the device yourself.
- Have a backup ventilation plan in place until your device is inspected or replaced.
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
606 units
Manufactured in
22002 26th Ave Se, Bothell, Washington, United States
Products
VC+Pro (Japan)
Model Number: PRT-00900-100, Package PN:PRT-00973-100. used for ventilatory support.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0125-2027More 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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