Skip to content
Recall Observatory FDA recall evidence

Device product

HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare System is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

Z-1131-2015

January 16, 2015

Class I

Product summary

Firm
HeartWare Inc
Event
Event 70340
Status
Terminated
Classification
Class I
Quantity
4,845
Official record key
device-enforcement:Z-1131-2015

Official wording

Reason: The affected clinical trial Controllers exhibit a higher susceptibility to ESD than newer commercial Controllers.

Code information: Product Codes- US product: Model No.: 1400, 1401US; International product: Model No.: 1400, 1401XX ('XX' represents country designation) Serial No.: CON000001 through CON005472

Distribution pattern: Worldwide Distribution - US Nationwide in the states of: AL, AZ, CA, CO, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, NC, NY, OH, OR, PA, TX, UT, VA, WA and District of Columbia and countries of: Canada, Poland, Australia, Austria, Italy, DE, New Zealand, South Africa, France, Switzerland, Germany, Brazil, UK, Belgium, Netherlands, Israel, Malaysia, Turkey, Greece, Japan, Singapore, Poland, Lithuania, Sweden, Norway, Finland, and India.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The affected clinical trial Controllers exhibit a higher susceptibility to ESD than newer commercial Controllers.