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FDA: Medtronic Guidewires High-Risk Recall

01/14/2014
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In December, the U.S. Food and Drug Administration (FDA) announced a recall of certain guidewires made by Medtronic, Inc. Patient complication reports were reported to the FDA and the company concerning the coating on the wire’s surface that had the potential to detach and delaminate. Medtronic began notifying hospitals and […]

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