Agency classClass IOur severity:Severe FDA (Devices)·Z-0132-2027·Announced 2026-10-28

Ventec V+ Pro Emergency Ventilator Recalled for Potential Connector Disconnection

Ventec Life Systems is recalling V+ Pro Emergency ventilators because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.

The agency’s classification

FDA (Devices): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as Class I because the internal cable connector may disconnect, potentially causing a system reboot and interruption of ventilation therapy. The source does not report any illnesses, injuries, or deaths.

Plain-English summary

Ventec Life Systems, Inc. is recalling the V+ Pro Emergency ventilator, Model Number PRT-01201-000. The recall involves 30,120 units distributed nationwide in the United States, including Puerto Rico. The product is identified by UDI 00855573007945 and package part numbers PRT-01173-000 and PRT-01222-000.

The recall is due to a defect where the ventilator's internal flow transducer cable connector may disconnect from the internal board. This disconnection can potentially result in a system reboot and an interruption of ventilation therapy.

The source text does not report any illnesses, injuries, or deaths associated with this defect. Consumers and healthcare facilities should contact Ventec Life Systems for instructions on how to address the issue.

The recalled product

Product: V+ Pro Emergency, Model Number: PRT-01201-000, Package PN:PRT-01173-000,PRT-01222-000. used for ventilatory support.
Manufacturer: Ventec Life Systems, Inc.
Category: Medical Device — Ventilator
Hazard: system-reboot
therapy-interruption
Affected units: 30,120

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

All Serial Numbers: UDI: 00855573007945

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Same manufacturer · Ventec Life Systems, Inc.

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Same hazard · system reboot