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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Timberline Anchored Lateral Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall EXp Tibial Insert Orthopedic Devices Stelkast Co 2 United States USFDA
Device Recall Aesculap Miethke Shunt System Neurological Devices Aesculap, Inc. 2 United States USFDA
Device Recall Stryker Orthopedics Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Hemostatic Bone Putty General and Plastic Surgery Devices Synthes, Inc. Unclassified United States USFDA
Device Recall MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm General and Plastic Surgery Devices Stryker Craniomaxillofacial Division 2 United States USFDA
Device Recall MEDPOR BARRIER Sheets Orbital Floor Implant General and Plastic Surgery Devices Stryker Craniomaxillofacial Division 2 United States USFDA
Device Recall MEDPOR BARRIER Sheets Rectangle General and Plastic Surgery Devices Stryker Craniomaxillofacial Division 2 United States USFDA
Device Recall MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPORTitaniumBarrier (MTB) Right General and Plastic Surgery Devices Stryker Craniomaxillofacial Division 2 United States USFDA
Device Recall Zimmer PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Itrel 3 IPG; InterStim II INS: InterStim INS ; Enterra INS Neurological Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SurgiWrap General and Plastic Surgery Devices MAST Biosurgery USA, Inc 2 United States USFDA
Device Recall Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Howmedica Osteonics Corp. LFT v40 Femoral Head Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker Howmedica Osteonics Triathlon Distal Capture Assembly Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall HeartWare Ventricular Assist System Cardiovascular Devices HeartWare Inc 3 United States USFDA
Device Recall HEMOCATH, SLX, PROPICC, VASCUPICC Gastroenterology-Urology Devices Medical Components, Inc dba MedComp 3 United States USFDA
Device Recall Telluride Percutaneous Rod Inserter Long Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Retractor Blade Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Set Screw Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 3 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 2 United States USFDA
Device Recall Mallory Head 4 Finned Acetabular Shell 50mm Orthopedic Devices Biomet, Inc. 2 United States USFDA