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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
Related Medical Device Recalls
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Z-0589-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-140BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0590-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-155BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0591-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-135BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0596-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-155BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0593-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-155BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0594-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-135BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0595-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-140BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
Z-0592-06 - Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-140BL 2 03/22/2006 FEI # 1000125107
Endologix Inc
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