[Recalled] Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare Ventricular Assist System (HVAD) is indicated in the United States (US) and European Union (EU) for use as a bridge to
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare Ventricular Assist System (HVAD) is indicated in the United States (US) and European Union (EU) for use as a bridge to cardiac transplantation (BTT) as well as an alternative to transplanta |
|---|---|
| Brand / manufacturer | Heartware, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0582-2019 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 19 November 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: HVAD Battery Charger units manufactured with wrong inductors.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Heartware, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.