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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Epix Universal Clip Applier General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall GK258, AME Standard Kit General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall GK213, AME Standard Kit General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Device Recall GK260, Standard Set General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA
Biliary Catheters Gastroenterology-Urology Devices Applied Medical Resources Corp 2 United States USFDA
Direct Drive Clip Applier General and Plastic Surgery Devices Applied Medical Resources Corp 2 United States USFDA