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MedPage Today on MSNTack 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 ...
Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
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Medical Device Network on MSNPhilips pulls endovascular implant from market after FDA Class I recall tagPhilips has recommended that customers immediately stop using affected Tack endovascular systems and return unused product to ...
Philips stopped selling its Tack endovascular system because of cases where additional interventions were needed to remove ...
This recall involves removing devices from use and sale. According to the FDA notice, the device may cause serious injury of ...
The FDA says user challenges and need for additional procedures drove recommendations to stop using the system immediately.
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 ...
The U.S. Food & Drug Administration said that Philips has removed and discontinued distribution of Tack Endovascular System ...
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 ...
Opens in a new tab or window The FDA said to stop all use of Philips' Tack Endovascular System, which is under class I recall for user difficulties in removing the device. The agency also ...
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