Class I is the most serious designation for a recall issued by the FDA. Image credit: Shutterstock / OleksSH. Philips will no longer sell its Tack endovascular system in the US following a Class I ...

March 6, 2025—The FDA advised this week that Philips is recalling the Tack endovascular systems because of challenges experienced by customers during use, including events where additional ...

Philips will no longer sell its Tack endovascular system in the US following a Class I recall by the US Food and Drug Administration (FDA). Class I is the most serious designation for a recall ...

The Food and Drug Administration has labeled a recall of Philips’ Tack Endovascular Systems as a Class l, which is the most serious kind of recall. There have been 20 reported injuries and no ...

According to a document from NHTSA, affected Evenflo car seats and travel systems were manufactured and may have been sold ...

More than 1,000 Evenflo car seats designed for the Canadian market were erroneously delivered to U.S. purchasers without the proper U.S. recall registration card. Twenty different car seat models ...

AMSTERDAM – With its recent clearance in France, the Sleep & Respiratory Care business at Philips can once again sell products in all countries except for the United States. “If you talk about S&RC, ...

Philips stopped selling an implant used to repair damaged arteries after reports of 20 injuries and some devices needing to be removed. The Food and Drug Administration said in a Monday recall notice ...