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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 20 Results
PMA Number: P040002
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Product Description
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Recall
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FDA Recall
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AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent G... 2 01/18/2017 Endologix
AFX Endovascular AAA System, Endoleak Type IIIB; The AFX Endovascular AAA System is intended for en... 2 01/18/2017 Endologix
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery Syst... 2 03/22/2006 Endologix Inc
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