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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 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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ENDOLOGIX AFX2 Bifurcated Endograft System, Stent Graft System, Rx Only, Sterile EO, REF: ... 1 10/03/2018 Endologix
ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22... 1 10/03/2018 Endologix
ENDOLOGIX AFX/AFX2, Limb (Iliac) Extension Endograft, Rx Only, Sterile EO, AFX Limb Accessory Model ... 1 10/03/2018 Endologix
ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Prox... 1 10/03/2018 Endologix
AFX Endovascular AAA System, Endoleak Type IIIB Common Name: AFX Bifurcated and Accessory Stent G... 2 01/19/2017 Endologix
AFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Accessory Stent ... 2 01/19/2017 Endologix
AFX Endovascular AAA System, Endoleak Type IIIA Product Usage: The AFX Endovascular AAA System i... 2 01/19/2017 Endologix
AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-0... 2 01/19/2017 Endologix
AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C7... 2 01/19/2017 Endologix
AFX Endovascular AAA System, Endoleak Type IIIA 2 01/18/2017 Endologix
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