Philips has recommended that customers immediately stop using affected Tack endovascular systems and return unused product to ...
Complications with the implant used to treat blood vessel dissection after balloon angioplasty or stent placement can result ...
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 ...
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 ...
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 ...
The FDA advised this week that Philips is recalling the Tack endovascular systems because of challenges experienced by customers d ...
It's made by a major brand in consumer electronics, but an unusual power issue may pose multiple dangers for many Americans.
The FDA said to stop all use of Philips' Tack Endovascular System, which is under class I recall for user difficulties in ...