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Recall Observatory FDA recall evidence

Device product

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.

Z-1698-2015

April 29, 2015

Class I

Product summary

Firm
HeartWare Inc
Event
Event 71164
Status
Ongoing
Classification
Class I
Quantity
3,747 currently implanted worldwide
Official record key
device-enforcement:Z-1698-2015

Official wording

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

Code information: Serial #: ALL HeartWare HVAD systems currently in use.

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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