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  • Device 2464
  • Manufacturer 541
  • Event 124969
  • Implant 1361
Name Classification Manufacturer Risk Class Country Source
Device Recall Trilogy Bone Screws Orthopedic Devices Zimmer Manufacturing B.V. 2 United States USFDA
Device Recall Osteobond Copolymer Bone Cement Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Persona Cemented Tibial Broach Inserter/Extractor Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Sirius Polish Cemented Stem 34B Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall SolitaireC Cervical Spacer System Orthopedic Devices Ebi, Llc 2 United States USFDA
Device Recall Timberline Anchored Lateral Retractable Drill Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Anchored Lateral Variable Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Anchored Lateral Retractable Sleeve Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Zimmer PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall PERSONA Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Telluride Percutaneous Rod Inserter Long Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Timberline Retractor Blade Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Set Screw Orthopedic Devices Biomet Spine, LLC 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 3 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 2 United States USFDA
Device Recall Mallory Head 4 Finned Acetabular Shell 50mm Orthopedic Devices Biomet, Inc. 2 United States USFDA
Device Recall Ringloc Acetabular Shell Limited Hole Finned 52mm Orthopedic Devices Biomet, Inc. 3 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 2 United States USFDA
Device Recall Zimmer Orthopedic Devices Zimmer Gmbh 3 United States USFDA
Device Recall Persona Trabecular Metal Tibial Plate / Persona TM Tibia Orthopedic Devices Zimmer, Inc. 2 United States USFDA
Device Recall NexGen Orthopedic Devices Zimmer Trabecular Metal Technology, 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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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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