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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 50 of 148 Results
Recall Date to: 10/01/2014 510(K) Number: K022947
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Product Description
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FDA Recall
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Roller Pump, 6 Inch Diameter The Terumo Advanced Perfusion System 1 is indicated for use for up t... 2 01/24/2012 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1- 6" Roller Pump for Terumo System 1 Product Usage: The Ter... 2 11/29/2011 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1- 4" Roller Pump for Terumo System 1 Product Usage: The Terumo... 2 11/29/2011 Terumo Cardiovascular Systems Corporation
Terumo Advanced Perfusion System 1- 6" Roller Pump for Terumo System 1 (gray) Product Usage: The... 2 11/29/2011 Terumo Cardiovascular Systems Corporation
The Terumo Advanced Perfusion System 1, Catalog Number 801763, System 1 Base, 110 V Product Usag... 2 11/29/2011 Terumo Cardiovascular Systems Corporation
The Terumo Advanced Perfusion System 1, Catalog Number 801764 System 1 Base, 220 V Product Usage... 2 11/29/2011 Terumo Cardiovascular Systems Corporation
Large Roller Pump 6" Diameter, Catalog 816571, Terumo Cardiovascular Systems, Corp., Ann Arbor, MI ... 2 07/06/2011 Terumo Cardiovascular Systems Corporation
System 1 Base 220V, Catalog 801764, Terumo Cardiovascular Systems, Corp., Ann Arbor, MI The prod... 2 07/06/2011 Terumo Cardiovascular Systems Corporation
System 1 Base 110V, Catalog 801763, Terumo Cardiovascular Systems, Corp., Ann Arbor, MI The prod... 2 07/06/2011 Terumo Cardiovascular Systems Corporation
Cardiovascular Procedure Kit, Part number 65871, Terumo Latin America Lactante Pack, Sterile, Terum... 2 06/22/2011 Terumo Cardiovascular Systems Corporation
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