Vista de la lista Vista de las tarjetas
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Smith and Nephew TWINFIX QUICKT Orthopedic Devices Smith & Nephew, Inc. 1 United States USFDA
Device Recall TWIST DRILL Cannulated Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall TWIST DRILL Cannulated Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall Normed VTEK TWIST DRILL Cannulated Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall Normed VTEK TWIST DRILL Cannulated Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall StealthStation System Orthopedic Devices Medtronic Navigation, Inc. 2 United States USFDA
Device Recall Surgical Instrument for SMR Anatomic and Reverse Shoulder Prosthesis Orthopedic Devices Limacorporate S.p.A 1 United States USFDA
Device Recall Light Adaptor for SBD & SBD II Orthopedic Devices The Anspach Effort, Inc. 1 United States USFDA
Device Recall Adaptor for SBD II Orthopedic Devices The Anspach Effort, Inc. 1 United States USFDA
Device Recall ROIA Anterior Delivery Device Orthopedic Devices LDR Spine USA, Inc. 1 United States USFDA
Device Recall Trident Universal Impactor/Positioner Orthopedic Devices Stryker Howmedica Osteonics Corp. 1 United States USFDA
Device Recall MANOS EX Orthopedic Devices Thayer Intellectual Property, Inc. 1 United States USFDA
Device Recall Synthes 0.76 mm Drill Bit Orthopedic Devices Synthes (USA) Products LLC 1 United States USFDA
Device Recall Carpel Tunnel Pack Surgical Instrument Tray Orthopedic Devices Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables 1 United States USFDA
Device Recall Dual Stylet Needle Orthopedic Devices Amendia, Inc 1 United States USFDA
Device Recall Stryker Orthopaedics Orthopedic Devices Stryker Howmedica Osteonics Corp. 1 United States USFDA
Device Recall DePuy Synthes orthopedic instruments Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Cannulated Drill bit 2.0mm and 2.6 mm Orthopedic Devices Flower Orthopedics Corporation 1 United States USFDA
Device Recall RIO THA System Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall Oxford Knee System Tibial Resector Body Tube & Guides Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA
Device Recall Oxford Partial Knee System Femoral Slap Hammer Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA
Device Recall Oxford Unicompartmental Knee Phase 3 Tibial Impactor Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA
Device Recall Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size A Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA
Device Recall Oxford Unicompartmental Knee Phase 3 Shim Size 3 Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA
Device Recall Oxford Unicompartmental Knee Phase 3 Shim Size 2 Orthopedic Devices Biomet U.K., Ltd. 1 United States USFDA