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# Ventec Life Recalls VOCSN Breathing Package
- URL: https://www.fdaweb.com/ventec-life-recalls-vocsn-breathing-package/
- Published: 2024-03-07T12:00:00.000Z
- Updated: 2026-09-14T14:24:45.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156510

Ventec Life Systems is recalling (Class 1) its VOCSN Patient Breathing Package due to a manufacturing issue that causes the bonded spiral wrap to detach before or during ventilation. “If the spiral wrap detaches, it can compromise the structural integrity, functionality, or cause blockage, stoppage, or leaks in the breathing circuit,” a [recall notice ](https://www.fda.gov/medical-devices/medical-device-recalls/ventec-life-systems-recalls-vocsn-patient-breathing-package-pediatric-active-oxygen-blue?utm%5Fmedium=email&utm%5Fsource=govdelivery)says.

The notice says that using an affected breathing package may cause serious injuries, such as failure to ventilate, incomplete ventilation, failure to oxygenate, and complete or partial airway obstruction. To date, there have been 15 complaints regarding the issue, and no injuries or deaths.

The device is intended to provide respiratory support for pediatric patients weighing at least 11 pounds, the agency says. It can be used at home, or in a medical clinic or hospital.