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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 45 Results
510(K) Number: K915183
 
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Perfusion System 8000, base 4 pump, 100V safety monitor included The Sarns" Modular Perfusion Sys... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 5 pump, 220V/240V safety monitor included The Sarns" Modular Perfusio... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 4 pump, 220V/240V safety monitor included The Sarns" Modular Perfusio... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 5 pump, 115V safety monitor included The Sarns" Modular Perfusion Sys... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns" Modular Perfusion Sys... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 5 pump, 100V safety monitor included The Sarns" Modular Perfusion Sys... 2 11/13/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 5 pump, 220V/240V safety monitor included The Sarns Modular Perfusion... 2 10/24/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion Syst... 2 10/24/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 5 pump, 115V safety monitor included The Sarns Modular Perfusion Syst... 2 10/24/2012 Terumo Cardiovascular Systems Corporation
Perfusion System 8000, base 4 pump, 220V/240V safety monitor included The Sarns Modular Perfusion... 2 10/24/2012 Terumo Cardiovascular Systems Corporation
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