Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...

This recall involves removing devices from use and sale. According to the FDA notice, the device may cause serious injury of ...

Philips stopped selling its Tack endovascular system because of cases where additional interventions were needed to remove ...

Philips has recommended that customers immediately stop using affected Tack endovascular systems and return unused product to ...

The U.S. Food & Drug Administration said that Philips has removed and discontinued distribution of Tack Endovascular System ...

The FDA says user challenges and need for additional procedures drove recommendations to stop using the system immediately.

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 ...

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 FDA said to stop all use of Philips' Tack Endovascular System, which is under class I recall for user difficulties in ...

Opens in a new tab or window Share on LinkedIn. 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 ...