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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 16 Results
Related Medical Device Recalls
 
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Z-0322-2007 - Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source required) base; Model 801763. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0333-2007 - Terumo Advanced Perfusion System 1 Flow Module; Catalog number 802018. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-324-2007 - Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0325-2007 - Terumo Advanced Perfusion System 1, 6 inch diameter Roller Pump; Model 801041. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0326-2007 - Terumo Advanced Perfusion System 1 Air Bubble Detection Module; Catalog number 802110. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0327-2007 - Terumo Advanced Perfusion System 1 Data Interface CDI 100; Catalog number 802558. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0328-2007 - Terumo Advanced Perfusion System 1 Data Interface CDI 500; Catalog number 803479. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0329-2007 - Terumo Advanced Perfusion System 1 Venous Occluder; Catalog number 803480. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0330-2007 - Terumo Advanced Perfusion System 1 Level Detection; Catalog number 802111. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
Z-0331-2007 - Terumo Advanced Perfusion System 1 Pressure Monitoring; Catalog number 802112. 2 12/30/2006 FEI # 1828100
Terumo Cardiovascular Systems Corp
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