FDA-Device2026-10-20Class IPROCESSING DEFECT

Ventec Life Systems V+Pro ventilator recalled for potential cable disconnection and therapy interruption

OTHERNationwide distributionMedical devices

What this means

The internal flow transducer cable connector in Ventec V+Pro ventilators may disconnect from the internal board. If this happens, the ventilator could reboot and temporarily stop delivering breathing support.

  • Check your V+Pro ventilator model number: PRT-01185-000, PRT-01185-001, or PRT-01185-002.
  • Contact Ventec Life Systems immediately for instructions or a replacement.
  • Do not stop using the device unless Ventec directs you to; continue following your doctor's care plan.
Get recalls like this in a free plain-English brief every Sunday.Get alerts ↓
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
39,568 units
Manufactured in
22002 26th Ave Se, Bothell, Washington, United States
Products
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.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0129-2027

More Ventec Life Systems recalls

Want us to check the next one for you?

We read every CPSC, FDA, USDA, and NHTSA notice and email you a plain-English Sunday brief covering your household — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Free · One email a week · Unsubscribe anytime
By signing up you agree to our Terms and Privacy Policy.