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 comes ...
Medtronic won CE mark for the Affera Sphere-360 catheter and completed the first cases of the device in the Horizon 360 IDE trial.
Providence-based Rhode Island Hospital saw an increase in external ventricular drain infections after switching to a Medtronic device that has since been recalled, the CDC said April 11. The hospital, ...
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 comes ...
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