Thoratec Corp. on Wednesday won U.S. approval to sell an implantable heart device as a permanent treatment for patients too sick for transplants, opening a new market for the product.

The FDA says the HeartMate products are being recalled due to a possible buildup of “biological material” that can obstruct the device and keep it from properly pumping blood. The accumulation ...

The FDA announced Monday that two heart pump products are being recalled after reports of ... Abbott Laboratories’ Thoratec Corp. is recalling 13,883 HeartMate II and HeartMate 3 Left ...

The FDA announced Monday that two heart pump products are being recalled after reports of ... Abbott Laboratories’ Thoratec Corp. is recalling 13,883 HeartMate II and HeartMate 3 Left ...

The FDA announced Monday that two heart pump products are being recalled after reports of 14 deaths and hundreds of injuries were associated with the devices. Skip to content. KHON2.

The FDA says the HeartMate products are being recalled due to a possible buildup of “biological material” that can obstruct the device and keep it from properly pumping blood. The accumulation ...

The FDA announced Monday that two heart pump products are being recalled after reports of ... Abbott Laboratories’ Thoratec Corp. is recalling 13,883 HeartMate II and HeartMate 3 Left ...

The Food and Drug Administration (FDA) announced Monday that two heart pump products are being recalled after reports of 14 deaths and hundreds of injuries were associated with the devices.

The FDA announced Monday that two heart pump products are being recalled after reports of 14 deaths and hundreds of injuries were associated with the devices.

The FDA says the HeartMate products are being recalled due to a possible buildup of “biological material” that can obstruct the device and keep it from properly pumping blood. The accumulation usually ...

The FDA announced Monday that two heart pump products are being recalled after reports of 14 deaths and hundreds of injuries were associated with the devices.