Food safety testing is not only required by regulating bodies, it helps prevent contaminated product from getting out the ...
While many people might leap at the chance of an adventure, deep sea scientist Dr María Belén Arias Mella was on holiday and ...
He was a vice president at the U.S. subsidiary of Gotion, a Chinese battery company that was trying to outcompete its peers ...
The FDA recall affects more than 25,000 of the Fridley-run company’s devices and follows reports of 17 injuries.
Despite a recall of three council members for the Colorado mountain town of Dillon, the development plan that put the wheels in motion for the recall effort will move forward. After the community ...
Boston Scientific has issued a recall of Accolade pacemaker devices, according to a safety communication from the U.S. Food and Drug Administration. The Accolade devices under recall include the ...
(Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic (NYSE:MDT)’s embolization device as "most serious", following reports of the deaths of four patients.
While the city council has agreed to move ahead with Porrit's plan, for now, should the recall pass for the three members of the council, Richard at least has sworn to slow things down ...
The devices are being recalled due to an increased risk for permanently entering Safety Mode. HealthDay News — Boston Scientific has issued a recall of Accolade pacemaker devices, according to a ...
FDA Classifies Recall of Medtronic Embolization Devices as 'Most Serious' (Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as ...
Do I have a say in this? I’m in Asheville all the time but live in Marshall. Just sayin’, look at the Boston disaster where they destroyed the city with an overhead highway and finally, at ...
Olympus has recalled endoscope guide sheath kits after receiving 26 reports of serious injuries linked to the devices. The Food and Drug Administration, which published a Class I recall notice ...