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Recall Observatory FDA recall evidence

Device product

HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX. 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. Designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

Z-0006-2017

August 17, 2016

Class I

Product summary

Firm
HeartWare, Inc
Event
Event 74999
Status
Ongoing
Classification
Class I
Quantity
344 pumps
Official record key
device-enforcement:Z-0006-2017

Official wording

Reason: Foreign material found within the driveline connector of the HVAD Pump that could cause increased impedance resulting in electrical faults.

Code information: All sterile un-implanted stock manufactured prior to HW25838 is subject to removal.

Distribution pattern: Worldwide Distribution - US, in the states of AL, AR, AZ, CA, DC, FL, IL, IN, KY, LA, MA, MI, MN, MO, NC, NE, NJ, NY, OH, OK, PA, SC, TX, UT, VA, and WI; and, the countries of Argentina, Belarus, Bosnia, Herzegovina, Brazil, Canada, Chile, Colombia, Hong Kong, India, Israel, Kazakhstan, Kuwait, Lebanon, Malaysia, New Zealand, Saudi Arabia, Serbia, Singapore, South Africa, South Korea, Taiwan, Turkey, and Vietnam.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    Foreign material