Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
Philips stopped selling its Tack endovascular system because of cases where additional interventions were needed to remove ...
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Tack System Recall; Gene Hackman's Pacemaker; Altitude and Valve Disease?Data from two French registries suggested that the need for reintervention after transcatheter aortic valve replacement was ...
Philips is pulling from the market an implant designed to help repair the interior of damaged blood vessels, following a serious product recall. | Philips is pulling from the market an implant ...
Philips has recommended that customers immediately stop using affected Tack endovascular systems and return unused product to ...
This recall involves removing devices from use and sale. According to the FDA notice, the device may cause serious injury of ...
Royal Phillips NV opted to withdraw the Tack endovascular repair device only six years after the U.S. FDA’s approved it. Tack is designed to repair vascular dissection caused by angioplasty. The ...
The FDA says user challenges and need for additional procedures drove recommendations to stop using the system immediately.
The U.S. Food & Drug Administration said that Philips has removed and discontinued distribution of Tack Endovascular System ...
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