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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Digitex 20 Polydioxanone (PDO) suture General and Plastic Surgery Devices Coloplast Manufacturing US, LLC 2 United States USFDA
Device Recall Restorelle DirectFix Posterior Mesh General and Plastic Surgery Devices Coloplast Manufacturing US, LLC 2 United States USFDA
Genesis Malleable Penile Prosthesis Gastroenterology-Urology Devices Coloplast Manufacturing US, LLC 2 United States USFDA
Kiwee ​​testicular prostheses and Vaginal stents Coloplast A/S Sweden SMPA
Rostorelle L, Polypropylene Mesh Obstetrical and Gynecological Devices Coloplast Manufacturing US, LLC 2 United States USFDA
Saline Filled Testicular Prosthesis Gastroenterology-Urology Devices Coloplast Manufacturing US, LLC 3 United States USFDA
Testicular Implant (Kiwee®) and Vaginal Stent Coloplast A/S Germany BAM
Titan OTR Inflatable Penile Prosthesis Gastroenterology-Urology Devices Coloplast Manufacturing US, LLC 3 United States USFDA
use of Vortek Single loop Ureteral Stents Coloplast A/S Germany BAM
Vortek™ ureteral stents Coloplast A/S Germany BAM
vortek Urethral stent Coloplast A/S Sweden SMPA