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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

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FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device

July 02, 2019

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

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Two Pediatric Cardiac Catheters Recalled for Defective Balloons

April 26, 2019

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