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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall PKG, HASSON CANNULA, 5.5MM, AUTOMATIC VALVE, STOP COCK Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MIXTER FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, HOOK SCISSORS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, HASSON CANNULA Stryker Endoscopy 2 United States USFDA
Device Recall PKG, FIXABLE CONE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, STRAIGHT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, CURVED, LONG Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BABY METZENBAUM SCISSORS, CURVED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MICRO SCISSORS, STRAIGHT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, 12.5/11MM 5.5 REDUCER Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BULLET FORCEPS, TAPERED, SERRATED, SPOON Stryker Endoscopy 2 United States USFDA
Device Recall PKG, LUERLOCK, MALE, 6MM TUBING Stryker Endoscopy 2 United States USFDA
Device Recall PKG, LUERLOCK, FEMALE, 6MM TUBING Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MARYLAND FORCEPS, CURVED, LEFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ROTATING HANDLE, RATCHET, INSULATED SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ROTATING HANDLE, RATCHET, INSULATED/SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ROTATING HANDLE, W/RATCHET, INSULATED SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, AXIAL HANDLE, W/RATCHET, INSULATED SHAFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, RING HANDLE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, SPRING HANDLE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ALLIS FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BABCOCK FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, NARROW JAW Stryker Endoscopy 2 United States USFDA
Device Recall PKG, PENNINGTON FORCEPS Stryker Endoscopy 2 United States USFDA