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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-1306-2025
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Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 1101... 1 03/13/2025 FEI # 1000116158
Medtronic Perfusion Systems
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