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  • Device 1211
  • Manufacturer 31827
  • Event 5885
  • Implant 4142
Name Classification Manufacturer Risk Class Country Source
Device Recall orthopedic tray Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall PREMIUM ARTHROSCOPY PK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall IMPLANTE DE ORTHOPEDIA Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall FEMORAL PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall HIP ORTHO. PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall SHOULDER PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall KNEE ARTHROSCOPY PK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall FEMORAL PACK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall SHOULDER ARTHROSCOPY PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall EXTREMITY ARM PACK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall SHOULDER PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall GOWN SURG. POLY REINF. XL XLONG Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall ARTHROSCOPY PACK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall HIP AND KNEE REPLACEMENT Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall EXTREMITY PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall SHOULDER PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall SHOULDER ARTHROSCOPY PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall REEMPLAZO DE RODILLA Y CADERA Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall SHOULDER PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall ORTHOPEDIC PACK BASIC Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall ARTHROSCOPY PK Orthopedic Devices Customed, Inc 2 United States USFDA
Device Recall ARTHROSCOPY SURGICAL PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall ORTHOIMPLANT SURGICAL PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall CARPAL TUNEL LARGE SURGICAL PACK Orthopedic Devices Customed, Inc 1 United States USFDA
Device Recall ARTHROSCOPY PACK 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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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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