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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 of 150 Results
510(K) Number: K022947
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Product Description
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Recall
Class
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System 1 Base 220/240V The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 ho... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
System 1 Base 100/120V The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 ho... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
System 1 Base 100/120V The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 ho... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
System 1 Base 220/240V. The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 h... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 System 1 Base, 220/240 V. The Terumo Advanced Perfusion Sys... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The electronic gas blender pr... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion Syst... 2 07/09/2012 Terumo Cardiovascular Systems Corporation
Central Control Module for System 1: System 1 Base, 100/120V The Terumo Advanced Perfusion System... 2 07/06/2012 Terumo Cardiovascular Systems Corporation
Central Control Module for System 1: System 1 Base, 220/240V The Terumo Advanced Perfusion System... 2 07/06/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 Base, 220/240V, Catalog 801764, 6 " Roller Pump Occlusion: Refer... 2 03/27/2012 Terumo Cardiovascular Systems Corporation
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