The correction is the latest recall that J&J’s Abiomed has issued in recent years for Impella devices and controllers.

The FDA issued an early alert related to a catheter introducer kit issue from Johnson & Johnson’s Abiomed Heart Recovery unit ...

Abiomed has initiated a voluntary recall for certain Automated Impella Controllers (AICs) used in conjunction with its Impella catheters following reports of one death as of 12 August in relation to a ...

There are new and revised warnings about the instructions for use of a certain type of heart pump that could lead to a risk of heart perforation, according to an alert issued by the pump's ...

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Certain Automated Impella Controllers (AICs), the main control interface for the Impella catheter (Abiomed/Johnson & Johnson MedTech), should not be used after another issue potentially affecting pump ...

Abiomed Inc. (NSDQ:ABMD) makes cardiac assist devices powerful enough to pump more than a gallon of blood through the heart each minute and small enough to be placed inside the heart via catheter.

isa Cardillo, then 36, and her husband were celebrating their 15th wedding anniversary and had just checked into a bed-and-breakfast when she felt a burning, stabbing pain in her chest. She was having ...

Abiomed is recalling all Impella left-sided blood pumps in the US over a potential safety issue when used in patients with a transcatheter aortic valve replacement (TAVR) stent ― something that is not ...