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 ...

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 ...

Passenger vans equipped with a brake warning indicator may have a power steering cooler hose that can separate from the power brake booster fluid flow witch assembly. If this occurs, power ...

KUALA LUMPUR, Feb 20 — The Road Transport Department (JPJ) has announced a recall involving 41,688 vehicles from six manufacturers due to potential structural, equipment, or system defects that could ...

RTD director-general Aedy Fadly Ramli said the recall is important to prevent accidents involving the vehicles. The vehicle models being recalled are Honda Civic and Honda CR-V, involving 36,678 ...