Z-2006-2012 Class I Terminated

Recalled by CareFusion 203, Inc. — Minneapolis, MN

Recall Details

Product Type
Devices
Report Date
July 25, 2012
Initiation Date
June 19, 2012
Termination Date
February 11, 2013
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
266

Product Description

CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum of 5 kg (11 lbs). It is suitable for service in hospital and transport environments as a source of continuous or intermittent positive pressure ventilatory support, delivered invasively or non-invasively. It is not intended for homecare use.

Reason for Recall

CareFusion identified that the EnVe Ventilator may not hold the set Positive End Expiratory Pressure (PEEP) value either intermittently or continuously or it may alarm for a Patient Circuit Fault. The unit will activate either a Low PEEP or Patient Circuit Fault Alarm both audibly and Visually to alert the healthcare professional. Ventilation delivery to the patient may be compromised.

Distribution Pattern

Nationwide Distribution including AZ, CA, CO, FL, IL, KY, ME, MI, MO, MN, MT, ND, NJ, NM, NV, NY, OK, PA, SC, SD, TX , UT, WI, and WV.

Code Information

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