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List view Cards view
  • Device 3026
  • Manufacturer 615
  • Event 124969
  • Implant 600
Name Classification Manufacturer Risk Class Country Source
Device Recall ACCOLADE TMZF PLUS HA 127 SIZE 0 HIP STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall AccuLIF Tubing Set Orthopedic Devices Stryker Spine 2 United States USFDA
Device Recall Asnis III Csnnulated Screw System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall AXSOS PLUS LOCKING PLATE SYSTEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Biosteon Orthopedic Devices Stryker Endoscopy 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CITATION TMZF HA STEM Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Collagen Meniscus Implant Orthopedic Devices Stryker Corporation 2 United States USFDA
Device Recall Corin Unipolar Adapter Sleeve Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall CuttingEdge Total Hip Instrumentation Surgical Protocol Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Dall Miles Cable Grip System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Distal Centralizer Exeter II Hip System Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall DURACON TOTAL KNEE SYSTEM TIBIAL COMPONENTS 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 External Compression Device Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall GAM Guide/Metaizeau Intramedullary Pin Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Gamma3 Orthopedic Devices Stryker Howmedica Osteonics Corp. 2 United States USFDA
Device Recall Gamma 3 Long Nail Kit R2.0 Orthopedic Devices Stryker Howmedica Osteonics Corp. 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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Disclaimer

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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