Ventec V+Pro Ventilators Recalled Due to Potential Internal Cable Disconnection
Ventec Life Systems is recalling V+Pro ventilators because an internal cable may disconnect, causing system reboots and interruption of 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 disconnection may interrupt ventilation therapy, posing a reasonable probability of serious adverse health consequences. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
Ventec Life Systems, Inc. is recalling V+Pro ventilators (Model Numbers PRT-01185-000, PRT-01185-001, and PRT-01185-002) used for ventilatory support. The recall involves 39,568 units distributed nationwide in the United States, including Puerto Rico.
The recall is being conducted because 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.
Healthcare facilities and users should contact Ventec Life Systems for instructions on how to address the defect. The source text does not report any illnesses, injuries, or deaths associated with this recall.
The recalled product
- Product
- 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.
- Manufacturer
- Ventec Life Systems, Inc.
- Category
- Medical Device — Ventilators
- Affected units
- 39,568
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 (3)
- All Serial Numbers: PRT-01185-000 -UDI: 00855573007877
- PRT-01185-001 - UDI: 00850018761161
- PRT-01185-002 - UDI: 00850018761154
Distribution
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