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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 07/05/2015
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Z-2104-2013 - Medtronic Custom Perfusion System. Model Numbers: 1D80R8, 1E34R1, 1F75R1, 1G49R2, 1G75R1, 1P07R8, 1P91R4, 5B15R11, and 5P51R9. Sterilized by Ethylene Oxide, Do no Reuse. Product Usage: Th... 2 08/27/2013 Medtronic Inc. Cardiac Rhythm Disease Management
Z-2106-2013 - Medtronic Custom Perfusion System with Trillium BioSurface (a polymer containing non-leaching heparin). Model Numbers: TL4X17R8, TL5D01R, TL5D02R, TL5D02R3, TL5D02R5, and TL6A65R7. Sterilized by ... 2 08/27/2013 Medtronic Inc. Cardiac Rhythm Disease Management
Z-2105-2013 - Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model Numbers: CB1D82R12 and CB5N73R7. Sterilized by Ethylene Oxide, Do no Reuse. Product Usage: Usage: This product is in... 2 08/27/2013 Medtronic Inc. Cardiac Rhythm Disease Management
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