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

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

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

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 ...

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.

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.

Philips this week announced it received EU MDR certification for remote scanning capabilities on its Radiology Operations ...

Philips CEO Roy Jakobs expects the subdued demand in China to continue in 2025, as tariffs also cause market uncertainty.