资讯

Shares of Medtronic (NYSE:MDT) reached a session low on Tuesday after the U.S. Food and Drug Administration (FDA) announced a product recall involving the company’s Pipeline Vantage 027 ...
March 18 (Reuters) - The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's (MDT.N), opens new tab embolization device as "most serious", following reports of the ...
The U.S. Food and Drug Administration on Tuesday announced a Class 1 recall — the most serious level — affecting more than 26,000 Medtronic devices used to treat brain aneurysms. The recall ...
The Food and Drug Administration on Tuesday classified Medtronic’s recall of its Pipeline Vantage embolization devices as the most serious type of recall. The recall removed Pipeline Vantage 027 ...
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 ...