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[Recalled] Heartware HVAD Pump Implant Kit, Product (REF) Number 1103 — The Outflow Graft may be subject to tears and the Strain Relief screw may break… | FDA 2020-04-03

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductHeartware HVAD Pump Implant Kit, Product (REF) Number 1103
Brand / manufacturerHeartware, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2055-2020
Country of noticeUnited States
Risk levelClass I
Hazard typerecall
Notice date03 April 2020
EAN / barcode00888707000017

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: The Outflow Graft may be subject to tears and the Strain Relief screw may break during the pre-implant pump assembly and attachment to the HVAD Pump.

This Class I 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

Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).

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.

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