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

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

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

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.

Medical device recalls surged last year, driven by stricter FDA oversight and a big jump in the most serious type of recalls.

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

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 ...

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 ...

With its recent clearance in France, the Sleep & Respiratory Care business at Philips can once again sell products in all ...