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Name Classification Manufacturer Risk Class Country Source
Device Recall Stryker T2 Femoral Nail System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Exeter Rasp/Trial Introducer/Extractor Handle part of the Exeter Femoral Hip System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker AccuLIF PL Cages Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker AccuLIF PL Cages Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker AccuLIF PL Cages Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Stryker LFIT Anatomic V40 Femoral Head Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall T2 K Wire Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall METS Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall METS Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall METS Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall METS Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall METS Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall JTS External Drive Unit (JTS Grower Drive) Orthopedic Devices Stanmore Implants Worldwide Ltd. 2 United States USFDA
Device Recall Collagen Meniscus Implant Orthopedic Devices Stryker Corporation 2 United States USFDA
Device Recall Accolade and Restoration hip product Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Accolade and Restoration hip product Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw Orthopedic Devices Stryker Corporation 2 United States USFDA
Device Recall Stryker AutoPlex System Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 2 United States USFDA
Device Recall Stryker WVAS Inflatable Vertebral Augmentation System Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 2 United States USFDA
Device Recall Triathlon Revision Knee Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Triathlon Revision Knee Orthopedic Devices Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Hinge Coupling Hoffmann LRF Orthopedic Devices Stryker GmbH 2 United States USFDA
Device Recall Stryker Orthopedic Devices Stryker Endoscopy 2 United States USFDA
Gamma3 Long Nail Kit, 120 degree, 11 x 320mm Right. And 125 degree Nail. Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
The TRIO Spondylolisthesis Reduction Instrument is a Class I Manual Surgical Instrument unique to the implantation of Stryker Spine TRIO PS this instrument is intended for use in the reduction of degenerative Spondylolisthesis. Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA