FDA-Device2026-10-20Class IPROCESSING DEFECT
Ventec Life Systems VC+Pro ventilator recalled for potential ventilation interruption
What this means
The internal flow transducer cable connector in Ventec VC+Pro ventilators (Model PRT-00900-001) may disconnect from the internal board. If this occurs, the ventilator could restart and temporarily stop delivering oxygen and ventilatory support to the patient.
- If you use or care for someone using a VC+Pro ventilator, contact Ventec Life Systems immediately for instructions.
- Do not attempt to repair or reseat the cable yourself.
- Have a backup ventilation plan in place until you receive guidance from Ventec or your clinician.
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
1,534 units
Manufactured in
22002 26th Ave Se, Bothell, Washington, United States
Products
VC+Pro
Model Number: PRT-00900-001, Package PN:PRT-00973-000. used for ventilatory support.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0124-2027More 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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