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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Z-2214-2026 - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2215-2026 - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2216-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2217-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2222-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2219-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2220-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2221-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
Z-2218-2026 - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter 2 05/20/2026 FEI # 1000116158
Medtronic Perfusion Systems
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