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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall HemosIL PTFibrinogen HS PLUS Hematology and Pathology Devices Instrumentation Laboratory Co. 2 United States USFDA
Device Recall PKG, BIPOLAR FORCEPS, FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIOPSY FORCEPS, SPOON Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIOPSY FORCEPS, SPOON W/PIN Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BLAKESLY BIOPSY FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BLAKESLY BIOPSY FORCEPS, SPOON W/PIN Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ATRAUMATIC FORCEPS, SINGLE ACTION Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION Stryker Endoscopy 2 United States USFDA
Device Recall PKG, SCHERTEL FORCEPS, FENESTRATED, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BLUNT FORCEPS, BLUNT, SERRATED, SPOON Stryker Endoscopy 2 United States USFDA
Device Recall PKG, DEBANEY FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG. MODIFIED 5X33 DEBAKEY Stryker Endoscopy 2 United States USFDA
Device Recall PKG, FUNDUS FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ALLIGATOR FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, COBRA FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, SERRSTED FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall 33CM DORSEY GRASPER FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, STRONG FORCEPS, FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BABCOCK FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, DELICATE, FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, ATRAUMATIC Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEP, BOWEL Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MICRO GRASPER Stryker Endoscopy 2 United States USFDA
Device Recall PKG, NEEDLE HOLDER, STRIAGHT, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, NEEDLE HOLDER, CURVED LEFT, Stryker Endoscopy 2 United States USFDA