FDA Enforcement Class I Ongoing

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205. Product Usage: For use as a bridge-to-cardiac transplantation in patient who are at risk of death from refractory end-stage left ventricular heart failure.

Recall: Z-1698-2015 · Reported June 17, 2015

Enforcement

Recall Number
Z-1698-2015
Event ID
71164
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
HeartWare Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Report Date
June 17, 2015
Initiation Date
April 29, 2015
Classification Date
June 8, 2015
Address
14400 Nw 60th Ave, N/A, Miami Lakes, FL, 33014-2807, United States

Description

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100, 1101,1102,1104,1104JP and 1205. Product Usage: For use as a bridge-to-cardiac transplantation in patient who are at risk of death from refractory end-stage left ventricular heart failure.

Reason

HeartWare has received complaints relating to damage or bent connection pins within the power supply ports of the VAD controller.

Code Info

Serial #: ALL HeartWare HVAD systems currently in use.

Distribution

Worldwide Distribution - US Nationwide in the states of AL, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OR, PA, SC, TN, TX, UT, VA and countries of Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Croatia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, India, Israel, Italy, Japan, Korea, Lebanon, Lithuania, Luxembourg, Malaysia, Netherlands, New Zealand, Norway, Poland, Romania, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Turkey, and UK.

Quantity

3,747 currently implanted worldwide