The FDA advised this week that Philips is recalling the Tack endovascular systems because of challenges experienced by customers d ...
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 ...
The FDA said to stop all use of Philips' Tack Endovascular System, which is under class I recall for user difficulties in ...
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 ...
Medical Device Network on MSN2d
Philips 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 ...
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 ...
With its recent clearance in France, the Sleep & Respiratory Care business at Philips can once again sell products in all ...
Medical device recalls surged last year, driven by stricter FDA oversight and a big jump in the most serious type of recalls.
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