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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall PKG, GRASPER FORCEPS, NARROW JAW Stryker Endoscopy 2 United States USFDA
Device Recall PKG, NEEDLE NOSE FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BIOPSY FORCEPS, PUNCH Stryker Endoscopy 2 United States USFDA
Device Recall Firefly General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Firefly General and Plastic Surgery Devices Intuitive Surgical, Inc. 2 United States USFDA
Device Recall Smiths Medical General Hospital and Personal Use Devices Smiths Medical ASD, Inc. 2 United States USFDA
Device Recall xcube and VTOMEX GE Inspection Technologies, LP Not Classified United States USFDA
Device Recall Smiths Medical General Hospital and Personal Use Devices Smiths Medical ASD, Inc. 2 United States USFDA
Device Recall Smiths Medical General Hospital and Personal Use Devices Smiths Medical ASD, Inc. 2 United States USFDA
Device Recall PKG, MYOMA DRILL Stryker Endoscopy 2 United States USFDA
Device Recall PKG, SCHERTEL FORCEPS, BLUNT FENESTRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, TROCAR, 8MM, PYRAMIDAL TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, TROCAR, 11MM, PYRAMIDAL TIP Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OBTURATOR, 11MM, FOR HASSON CANNULA, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, CANNULA Stryker Endoscopy 2 United States USFDA
Device Recall Lite DM (Lite Data Manager) General Hospital and Personal Use Devices Horiba Instruments Inc 1 United States USFDA
Device Recall Aquillion One TSX301A/2D Radiology Devices Toshiba American Medical Systems Inc 2 United States USFDA
Device Recall Handy Laser Compact Laser centering GE Inspection Technologies, LP Not Classified United States USFDA
Device Recall TomoTherapy Radiology Devices TomoTherapy Incorporated 2 United States USFDA
Device Recall UniStrip1 Clinical Chemistry and Clinical Toxicology Devices Unistrip Technologies LLC 2 United States USFDA
Device Recall Maquet Datascope, Corp. Inc. Cardiovascular Devices Maquet Datascope Corp - Cardiac Assist Division 2 United States USFDA
Device Recall Captia (TM) Syphilis IgM Capture Immunology and Microbiology Devices Clark Laboratories, Inc. (dba,Trinity Biotech USA) 2 United States USFDA
Device Recall Sensei X Robotic Catheter System Cardiovascular Devices Hansen Medical Inc 2 United States USFDA
Device Recall NexGen Complete Knee Solution Monoblock Tibial Provisional/Drill Guide Orthopedic Devices Zimmer Trabecular Metal Technology, Inc. 1 United States USFDA
Device Recall PKG, PALPATION PROBE GRADUATED Stryker Endoscopy 2 United States USFDA