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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K182586
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Medtronic Cardioplegia Adapters: a) DLP® 1.8 m (6 ft) Pressure Monitoring Extension Line Adapter,... 2 05/10/2024 Medtronic Perfusion Systems
Medtronic Aortic Root Cannulae and Cardioplegia Needles: a) DLP® 9 Ga (11 Fr) Aortic Root Cannula... 2 05/10/2024 Medtronic Perfusion Systems
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