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.

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

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

Philips on Wednesday posted worse-than-expected losses in 2024, as the Dutch medical device maker bids to turn the page on a damaging recall of faulty sleep machines. For the fourth quarter, Philips ...