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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
Class
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FDA Recall
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ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Prox... 1 10/03/2018 Endologix
ENDOLOGIX AFX2 Bifurcated Endograft System, Stent Graft System, Rx Only, Sterile EO, REF: ... 1 10/03/2018 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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