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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K860149
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Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmo... 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary... 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonar... 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmona... 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
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