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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-2811-2026
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EOPA 3D Arterial Cannula 22FR, intended for use with cardiopulmonary bypass as an arterial return ca... 2 07/27/2026 FEI # 1000116158
Medtronic Perfusion Systems
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