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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 150 Results
Recall Date to: 07/29/2015 510(K) Number: K022947
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Product Description
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FDA Recall
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Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion Syst... 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 System 1 Base, 220/240V. The Terumo Advanced Perfusion Syst... 2 07/13/2012 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 (4 inch diameter Roller Pump, Gray; Model 816570). Extracorpor... 2 12/11/2008 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 (4 inch diameter Roller Pump; Model 801040). Extracorporeal ci... 2 12/11/2008 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 (6 inch diameter Roller Pump, Gray; Model 816571). Extracorpor... 2 12/11/2008 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 (6 inch diameter Roller Pump; Model 801041). Extracorporeal ci... 2 12/11/2008 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1 (with 4 inch diameter roller pump); Catalog number 801040. 2 03/31/2005 Terumo Cardiovascular Systems Corp
Terumo Advanced Perfusion System 1 (with 6 inch diameter roller pump); Catalog number 801041. 2 03/31/2005 Terumo Cardiovascular Systems Corp
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