Class 1 Recall: HeartWare Recalls Ventricular Assist Device Controllers Due to Loose Connectors which may Prevent Alarm from Sounding and Pump Stops
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
The HVAD helps deliver blood from the heart to the rest of the body. It is used in patients who are at risk of death from end-stage left ventricular heart failure and who are waiting for a heart transplant. The system includes a pump implanted in the space around the heart (pericardium) and a controller that controls the speed and function of the pump.
The HVAD is designed for use both in and out of hospital settings, including during patient transport.
Reason for Recall
HeartWare Inc. is recalling the HVAD controller due to a loose power connector which may cause the rear portion of the pump's driveline connector to become separated from the front portion of the driveline connector. A loose connector may allow moisture to enter the controller causing corrosion, electrical issues, reduced speaker volume and connection failures. If the speaker volume is decreased, the patient may not hear the alarm. If there is a loss of connection, the pump may stop which could cause serious adverse health consequences, including death.
HeartWare issued a related recall for the HVAD on July 29, 2016.
Who May be Affected
What to Do
On June 8, 2016, HeartWare Inc. sent an "Urgent Medical Device Correction" letter to affected customers. The letter instructed providers who care for these patients to:
Health care providers who have questions should contact their HeartWare representative or contact HeartWare Inc. at email@example.com or 1-877-367-4823 with any questions related to this recall.
Date Recall Initiated:
February 29, 2016