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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. For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure.

Z-1731-2015

April 29, 2015

Class I

Product summary

Firm
HeartWare Inc
Event
Event 71239
Status
Ongoing
Classification
Class I
Quantity
3,747 curently implanted
Official record key
device-enforcement:Z-1731-2015

Official wording

Reason: Complaints with the HVAD Internal Controller Alarm Battery failures.

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

Distribution pattern: Worldwide Distribution -- US, including 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, and VA; and, the 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

    Complaints with the HVAD Internal Controller Alarm Battery failures.