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  • Device 1211
  • Manufacturer 31827
  • Event 5885
  • Implant 4142
Name Classification Manufacturer Risk Class Country Source
Device Recall Synthes Electric Pen Drive (EPD) System Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall Brainlab AG Orthopedic Devices Brainlab AG 2 United States USFDA
Device Recall System 6 Aseptic Housing Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 1 United States USFDA
Device Recall Robotic Arm Interactive Orthopedic System (RIO) Orthopedic Devices Mako Surgical Corporation 2 United States USFDA
Device Recall KYPHON(R) EXPRESS(TM), Osteo Introducer(R) System, Diamond and Bevel, Size 2 Orthopedic Devices Medtronic Sofamor Danek USA Inc 1 United States USFDA
Device Recall Synthes Inserter for Titanium Elastic Nails Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall RECLAIM Revision Hip System; Assembled Implant Inserter Adaptor Orthopedic Devices DePuy Orthopaedics, Inc. 1 United States USFDA
Device Recall Reamers Orthopedic manual surgical instrument Orthopedic Devices Captiva Spine, Inc 1 United States USFDA
Device Recall Instrument Kit for use with OsteoSponge SC grafts Orthopedic Devices Bacterin International, Inc. 1 United States USFDA
Device Recall Lineum HF Torque Handle Limit (Lineum) Orthopedic Devices Biomet Spine, LLC 1 United States USFDA
Device Recall Torque Limiting Handle (Aspen/ Alpine) Orthopedic Devices Biomet Spine, LLC 1 United States USFDA
Device Recall Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 Orthopedic Devices The Anspach Effort, Inc. 1 United States USFDA
Device Recall Stryker Instruments Orthopedic Devices Stryker Instruments Div. of Stryker Corporation 1 United States USFDA
Device Recall Zimmer Anatomical Shoulder Handle for Rasp Orthopedic Devices Zimmer Gmbh 1 United States USFDA
Device Recall Cannulated Drill Bits Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall Optigun Ratchet Orthopedic Devices BIOMET FRANCE S.A.R.L. 1 United States USFDA
Device Recall Reamer / Irrigator / Aspirator (RIA) Orthopedic Devices Synthes, Inc. 1 United States USFDA
Device Recall Oxford Fixed Lateral Orthopedic Devices Biomet, Inc. 1 United States USFDA
Device Recall Musculoskeletal Transplant Foundation Allofix Insertion Kit Orthopedic Devices Musculoskeletal Transplant Foundation, Inc. 1 United States USFDA
Device Recall Orthopedic saw blade Orthopedic Devices EXP Pharmaceutical Services Corp 1 United States USFDA
Device Recall Femoral Cut Block Orthopedic Devices Encore Medical, Lp 1 United States USFDA
Device Recall S4C Occiput Torque Wrench F/Set Screw Orthopedic Devices Aesculap, Inc. 1 United States USFDA
Device Recall 8.5mm Reamer Head for Flexible Intramedullary Nailing System Orthopedic Devices Synthes (USA) Products LLC 1 United States USFDA
Device Recall ARTHROSCOPY PACK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall ARTHROSCOPY PK Orthopedic Devices Customed, Inc 2 United States USFDA
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About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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