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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall CSA Medical truFreeze Console General and Plastic Surgery Devices CSA Medical 2 United States USFDA
Device Recall Light Sheer Desire Diode Laser System with XC Handpiece Accessory options General and Plastic Surgery Devices Lumenis Limited 2 United States USFDA
Device Recall Amerigel General and Plastic Surgery Devices Amerx Health Care Corp. Unclassified United States USFDA
Device Recall Gyrus ACMI Diego Elite Tubeset General and Plastic Surgery Devices Gyrus Acmi, Incorporated 2 United States USFDA
Device Recall Gyrus ACMI Diego Elite Tubeset General and Plastic Surgery Devices Gyrus Acmi, Incorporated 2 United States USFDA
Device Recall Manual General Surgery Drill Guide General and Plastic Surgery Devices Orthofix, Inc 1 United States USFDA
Device Recall American Catheter 9100 Series General and Plastic Surgery Devices American Catheter Corp 1 United States USFDA
Device Recall ActCel Topical Hemostatic Dressing General and Plastic Surgery Devices Coreva Health Science LLC Unclassified United States USFDA
Device Recall da Vinci S and Si Surgical System General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Beaver Visitec International, Inc. General and Plastic Surgery Devices Beaver-Visitec International Inc. 2 United States USFDA
Device Recall SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP General and Plastic Surgery Devices Symmetry Surgical, Inc. 1 United States USFDA
Device Recall LapSac Surgical Tissue Pouch General and Plastic Surgery Devices Cook Inc. 1 United States USFDA
Device Recall EVac 70 XTRA with Integrated Cable General and Plastic Surgery Devices ArthroCare Medical Corporation 2 United States USFDA
Device Recall PROcise XP Wand with Integrated Cable General and Plastic Surgery Devices ArthroCare Medical Corporation 2 United States USFDA
Device Recall Beaver Visitec International, Inc General and Plastic Surgery Devices Beaver-Visitec International Inc. 2 United States USFDA
Device Recall Beaver Visitec International, Inc General and Plastic Surgery Devices Beaver-Visitec International Inc. 2 United States USFDA
Device Recall Beaver Visitec General and Plastic Surgery Devices Beaver-Visitec International Inc. 2 United States USFDA
Device Recall Beaver Visitec General and Plastic Surgery Devices Beaver-Visitec International Inc. 2 United States USFDA
Device Recall StoneLight 30 Laser System (NS3000) General and Plastic Surgery Devices New Star Lasers, Inc. 2 United States USFDA
Device Recall PowerLED, XTEN, and VOLISTA Surgical Light Systems General and Plastic Surgery Devices Maquet Cardiovascular Us Sales, Llc 2 United States USFDA
Device Recall Pull Reduction Device For 4.3mm Percutaneous Drill Guide General and Plastic Surgery Devices Synthes, Inc. 1 United States USFDA
Device Recall SERFAS 90 degree Energy Probe, Part Number 279350101 General and Plastic Surgery Devices Stryker Endoscopy 2 United States USFDA
Device Recall Natrelle General and Plastic Surgery Devices Allergan Inc Unclassified United States USFDA
Device Recall Maquet Inc. Hybrid OR Table General and Plastic Surgery Devices Maquet Cardiovascular Us Sales, Llc 1 United States USFDA
Device Recall INSTRUMENT ARM DRAPE, IS4000, 20 PACK General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA