Ventec V*Home Ventilator Recalled for Potential Flow Transducer Cable Disconnection
Ventec Life Systems is recalling V*Home ventilators because an internal cable connector 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 flow transducer cable connector may disconnect, potentially interrupting ventilation therapy. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
Ventec Life Systems, Inc. is recalling V*Home ventilators, Model Number PRT-01444-000, Package PN PRT-01445-000. The recall involves 25,112 units distributed nationwide in the United States, including Puerto Rico. The product is used for ventilatory support.
The recall is being issued 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.
The source text does not report any illnesses, injuries, or deaths associated with this defect. Consumers should contact Ventec Life Systems for further instructions regarding the recall.
The recalled product
- Product
- V*Home, Model Number: PRT-01444-000, Package PN:PRT-01445-000. used for ventilatory support.
- Manufacturer
- Ventec Life Systems, Inc.
- Category
- Medical Device — Ventilator
- Affected units
- 25,112
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: 00855573007822
Distribution
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