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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1000-2014
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Medtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Cannulae. Mod... 2 02/20/2014 FEI # 2182208
Medtronic Inc. Cardiac Rhythm Disease Management
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