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

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 ...

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

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 ...

Medical device recalls surged last year, driven by stricter FDA oversight and a big jump in the most serious type of recalls.

Ahead of Arsenal’s clash with PSV tonight, recall when Arsene Wenger’s side were reduced to nine men in Eindhoven in 2004… ...

With its recent clearance in France, the Sleep & Respiratory Care business at Philips can once again sell products in all ...

Data from two French registries suggested that the need for reintervention after transcatheter aortic valve replacement was ...

A Coastguard official broke down as he described taking a "distressing" phone call during the Channel's deadliest migrant ...