FDAJune 25, 2024device

HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant Kits or distributed separately: HeartMate 3 LVAS Implant Kit, US, Model: 106524US; HeartMate 3 LVAS Implant Kit, OUS, Model: 106524INT; HeartMate 3 System Controller, US, Model: ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Left ventricular assist system controller UI membrane/screen may lift along the edge of the controller housing, and if controller is exposed to fluid, ingress may occur, which may damage printed circuit board assemblies, which could result in unexpected and false positive alarms, loss of visual alarms, loss of user interface(use of buttons, loss of visual alarms,etc.), loss of power, and pump stop

What to do

FDA enforcement status: Ongoing

Brands named

thoratec

UPCs

0081302401329700813024011712008130240132350081302401184205415067031105

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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