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

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

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.

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

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

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

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 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 ...