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The FDA recall notification advised that all customers should stop using the Tack endovascular system immediately and that Philips will no longer distribute the system for use. According to the ...
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 ...
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 ...
Philips is pulling from the market an implant designed to help repair the interior of damaged blood vessels following a serious product recall. The company’s Tack endovascular system includes a ...
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 ...
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 ...
[Image from Philips] The FDA has deemed a recall of the Philips (NYSE: PHG) + Tack endovascular system Class I, the most serious kind. This recall involves removing devices from use and sale.
Philips is recalling the Tack endovascular system because of what it says are user challenges that have led to additional interventions needed to retrieve or remove the implant. The US Food and Drug ...