HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit side).
Recall
- Recall Number
- Z-1832-2017
- Event Number
- 76807
- Firm
- Heartware
- FEI Number
- 3007042319
- Product Code
- DSQ
- Status
- Open, Classified
- Root Cause
- Device Design
- Initiated
- March 10, 2017
- Address
- 14400 NW 60th Ave, Miami Lakes, FL, 33014-2807
Description
HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit side).
In April 2015, HeartWare, now a part of Medtronic, notified users of a safety issue related to the HVAD Pump Driveline Splice Kit. Medtronic now intends to send a follow-up communication to identified clinicians informing them that a new, improved splice kit is available.
HeartWare, now a part of Medtronic sent an Urgent Medical Device Recall letter on April 2015 and a follow-up letter on March 2017, to customers via overnight mail and/or email.. The letters identified the affected product, problem and actions to be taken. Customers were instructed to review the recall notice, forward the notice to individuals within their organization who need to be aware of the notice, complete, sign, and return the Acknowledgement Form . For questions contact your local HeartWare representative.
Worldwide Distribution - US Nationwide in the states of FL, MO, TN, KY, NY and the country of Germany.
9 units