Endologix: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: January 25, 2017. Most recent: October 10, 2018.

Risk classification: Class I: 1 · Class II: 7

Most recent recalls

DateAgencyProduct
October 10, 2018FDAENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, …Z-0008-2019
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type IIIA Product Usage: The AFX Endovascular A…Z-1047-2017
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Acces…Z-1039-2017
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type IIIAZ-1035-2017
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Access…Z-1037-2017
January 25, 2017FDAAFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-4…Z-1049-2017
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type IIIB Common Name: AFX Bifurcated and Access…Z-1054-2017
January 25, 2017FDAAFX Endovascular AAA System, Endoleak Type IIIB; The AFX Endovascular AAA System is inte…Z-1038-2017

Questions about this company

How many recalls does Endologix have?
Recalert has 8 U.S. recalls on record for Endologix, published between January 25, 2017 and October 10, 2018.
What was the most recent Endologix recall?
FDA recall Z-0008-2019, published October 10, 2018: ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Proximal Accessory, Infrarenal Model #/REF: A22-22/C55, A22-22/C75, A22-22/C95, A25-25…
Which agencies have handled Endologix recalls?
Endologix appears as the recalling firm in recalls from: FDA (8).

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