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 advised this week that Philips is recalling the Tack endovascular systems because of challenges experienced by customers d ...

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 designed ...

It's made by a major brand in consumer electronics, but an unusual power issue may pose multiple dangers for many Americans.

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 ...