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

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

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 ...

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 ...

An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Uncle Nicko ...

Philips is recalling the software associated with its mobile cardiac outpatient telemetry devices after 109 patient injuries and two patient deaths, a Jan. 13 FDA recall notice said. The software ...

Philips has posted 33.6% higher losses for 2024 compared to 2023 as the company continues to battle weaker demand in China and settlements for its faulty sleep apnoea devices. Philips reported ...