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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Wound Management Ltd. TOPPER Xtra Absorbent Dressing Pads Systagenix Wound Management Ltd. Hong Kong DH
V.A.C. GranuFoam Silver Dressing General and Plastic Surgery Devices KCI USA, Inc. 2 United States USFDA
TOPPER Xtra Absorbent Dressing Pads, Sterile KCI Medical Australia Pty Ltd Australia DHTGA
TOPPER Xtra Absorbent Dressing Pad Model: M11121N,Ml1131,Mlll41,P55263,P55264,P55255 Systagenix Wound Management Switzerland SATP
TOPPER Xtra Absorbent Dressing Pad Systagenix Wound Management Denmark DMA
Topper Xtra absorbent Systagenix France ANSM
Tielle S Hydrocell Dressing Systagenix Wound Management Limited France ANSM
the TOPPER® Xtra Absorbent Dressing Pads Systagenix Wound Management Germany BAM
RELEASE* Non-Adherent Absorbent Dressing Systagenix Ireland HPRA
Negative Pressure Wound Therapy Systems General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
KCI Prevena Incision Management System KCI USA Inc New Zealand NZMMDSA
Device Recall PRE2055US: Prevena Customizable Dressing 5Pack (USONLY) General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE2055: Prevena Customizable Dressing 5Pack General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE2001US: Prevena Incision Management Customizable System Box (USONLY) General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE2001: Prevena Incision Management Customizable System Box General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE1055US: Prevena Dressing, 5 Pack (USONLY) General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE1055: Prevena Dressing, 5 Pack General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE1001US: Prevena Peel and Place System Kit (USONLY) General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall PRE1001: Prevena Peel and Place System Kit General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
Device Recall CelluTome General and Plastic Surgery Devices KCI USA, Inc. 1 United States USFDA
Device Recall CelluTome General and Plastic Surgery Devices KCI USA, INC. 1 United States USFDA
Device Recall ActiV.A.C. 300ml Canister (with Gel) for ActiV.A.C. Therapy System General and Plastic Surgery Devices KCI USA, INC. 2 United States USFDA
ArjoHuntleigh BariAir Therapy System KCI USA Inc New Zealand NZMMDSA
500ml Canister/InfoV.A.C. KCI Germany BAM
300mL Canister (with Gel) for use with the ActiV.A.C. Therapy System KCI Medical Australia Pty Ltd Australia DHTGA