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Name Classification Manufacturer Risk Class Country Source
Device Recall TigerPaw System II General and Plastic Surgery Devices Laax, Inc. 2 United States USFDA
Device Recall TigerPaw System II General and Plastic Surgery Devices Laax, Inc. 2 United States USFDA
Device Recall iCAST and Advanta Anesthesiology Devices Atrium Medical Corporation 2 United States USFDA
Device Recall ProLite Mesh General and Plastic Surgery Devices Atrium Medical Corporation 2 United States USFDA
Device Recall HEMASHIELD Knitted Double Velour Cardiovascular Fabric Cardiovascular Devices GETINGE US SALES LLC 2 United States USFDA
the TIGERPAW System II General and Plastic Surgery Devices LAAx Inc. Germany BAM
Atrium Advanta V12 Covered Stent Atrium Medical Corporation Merrimack Germany BAM
HemaCarotid Knitted Ultra Thin Patch InterVascular Germany BAM
HemaCarotid Patch ultrathin knitted InterVascular S.A.S. Germany BAM
InterGard Knitted vascular graft Intervascular S.A.S. Germany BAM
"Exxcel Soft Standard Wall Vascular Graft" MAQUET Germany BAM
vascular prosthesis InterGard Knitted Heparin InterVascular Germany BAM
TIGERPAW System II General and Plastic Surgery Devices LAAx Inc Sweden SMPA
Device Recall Advanta VXT Vascular Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Flixene IFG Vascular Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Advanta SuperSoft Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Flixene IFG with Assisted Delivery Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Advanta SST Bifurcated Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Advanta VS Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Advanta VXT Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall Advanta SST Grafts Cardiovascular Devices Atrium Medical Corporation 2 United States USFDA
Device Recall CQUR Mesh General and Plastic Surgery Devices Atrium Medical Corporation 2 United States USFDA
Device Recall CQUR Edge Mesh General and Plastic Surgery Devices Atrium Medical Corporation 2 United States USFDA
Device Recall CQUR VPatch Mesh General and Plastic Surgery Devices Atrium Medical Corporation 2 United States USFDA
Device Recall CQUR TacShield Mesh General and Plastic Surgery Devices Atrium Medical Corporation 2 United States USFDA