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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 148 Results
Recall Date to: 08/08/2014 510(K) Number: K022947
 
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The Terumo Advanced Perfusion System 1, Catalog Number 801764 System 1 Base, 220 V Product Usage... 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
Terumo® Advanced Perfusion System 1: 100/120V AC, Advanced Perfusion System 1 The Terumo® Advance... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1: 220/240V AC, Advanced Perfusion System 1 The Terumo® Advanc... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 (APS1, System 1) Description: 220/240V AC Product Usage: Th... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 (APS1, System 1) 100/120V AC Product Usage: The Terumo® Adv... 2 08/14/2013 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 220/240V AC, Advanced Perfusion System Platform (APS) 2 07/08/2014 Terumo Cardiovascular Systems Corporation
Terumo® Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS) 2 07/08/2014 Terumo Cardiovascular Systems Corporation
Terumo ultrasonic air sensor, 1/4" by 1/16" (6.4 mm x 1.6 mm), Black, for use on Terumo perfusion sy... 2 01/24/2008 Terumo Cardiovascular Systems Corp
Terumo Ultrasonic air sensor, 3/8" by 3/32" (9.5 mm x 2.4 mm), Red, for use on Terumo perfusion syst... 2 01/24/2008 Terumo Cardiovascular Systems Corp
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