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Name Classification Manufacturer Risk Class Country Source
Synthes Spiral Blade Component of the Synthes Modular Blade Plate System Orthopedic Devices Synthes USA (HQ), Inc. United States USFDA
Device Recall Discovery XR656 Orthopedic Devices GE Healthcare, LLC United States USFDA
Device Recall Triathlon PKR Peg Drill Orthopedic Devices Stryker Howmedica Osteonics Corp. United States USFDA
CPT Modular Stem Orthopedic Devices Zimmer, Inc. United States USFDA
CPT Modular Stem Orthopedic Devices Zimmer, Inc. United States USFDA
Ascension PIP Orthopedic Devices Ascension Orthopedics, Inc United States USFDA
Ascension MCP Orthopedic Devices Ascension Orthopedics, Inc United States USFDA
Spine Wave Orthopedic Devices Spine Wave Inc United States USFDA
Device Recall Hip Prostheses Orthopedic Devices Ortho Development Corporation United States USFDA
Device Recall Hip Prostheses Orthopedic Devices Ortho Development Corporation United States USFDA
Device Recall Hip Prostheses Orthopedic Devices Ortho Development Corporation United States USFDA
Device Recall Hip Prostheses Orthopedic Devices Ortho Development Corporation United States USFDA
Stryker Advanced Cement Mixing System Bowl and 180 Gram Cement Cartridge with Break-Away Femoral Nozzle for use with Stryker high vacuum cement injection system, 6 pack; part 0306-563-000. Orthopedic Devices Stryker Instruments, Instruments Div. United States USFDA
Device Recall Mitek Products Orthopedic Devices Mitek Worldwide United States USFDA
Device Recall Mitek Products Orthopedic Devices Mitek Worldwide United States USFDA
Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF***QTY 1 BioScrew XtraLok ***STERILE***Linvatec, LINVATEC CORPORATION LARGO, FL 33773 USA***''. Orthopedic Devices Linvatec Corp. United States USFDA
Plus Orthopedics Orthopedic Devices Plus Endoprothetik AG United States USFDA
Device Recall Rotating Cutter Orthopedic Devices Orthofix, Inc. United States USFDA
Device Recall ATTUNE INTUITION Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Mandible Locking Plate (MLP) Bender / Cutter Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall POWEREASE(TM) Instruments Set Screw Breakoff Instrument Orthopedic Devices Medtronic Sofamor Danek USA Inc 1 United States USFDA
Device Recall Fixed Tibial bearing ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Rotating Tibial Platform ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Femoral Impactor ATTUNE INTUITION Impactor Orthopedic Devices DePuy Orthopaedics, Inc. 1 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