{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mercedita",
      "state": "PR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72900",
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "address_1": "Turpeaux Industrial Park Rd 1 km 123.4",
      "address_2": "",
      "postal_code": "00715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1144-2016",
      "product_description": "Product 46 consists of all product under  product code: HWC and same usage:  Item no:\t  114204012\tMINI MAGNA-FX CANN SCREW  114204016\tMINI MAGNA-FX CANN SCREW  114204020\tMINI MAGNA-FX CANN SCREW  114204024\tMINI MAGNA-FX CANN SCREW  114204028\tMINI MAGNA-FX CANN SCREW  114204032\tMINI MAGNA-FX CANN SCREW  114204036\tMINI MAGNA-FX CANN SCREW  114204040\tMINI MAGNA-FX CANN SCREW  114204044\tMINI MAGNA-FX CANN SCREW  114204048\tMINI MAGNA-FX CANN SCREW  114204055\tMINI MAGNA-FX CANN SCREW  114204065\tMINI MAGNA-FX CANN SCREW  114204124\tMINI MAGNA-FX CANN SCREW  114204126\tMINI MAGNA-FX CANN SCREW  114204128\tMINI MAGNA-FX CANN SCREW  114204130\tMINI MAGNA-FX CANN SCREW  114204132\tMINI MAGNA-FX CANN SCREW  114204134\tMINI MAGNA-FX CANN SCREW  114204136\tMINI MAGNA-FX CANN SCREW  114204138\tMINI MAGNA-FX CANN SCREW  114204140\tMINI MAGNA-FX CANN SCREW  114204142\tMINI MAGNA-FX CANN SCREW  114204144\tMINI MAGNA-FX CANN SCREW  114204146\tMINI MAGNA-FX CANN SCREW  114204148\tMINI MAGNA-FX CANN SCREW  114204150\tMINI MAGNA-FX CANN SCREW  114204155\tMINI MAGNA-FX CANN SCREW  114204160\tMINI MAGNA-FX CANN SCREW  114204165\tMINI MAGNA-FX CANN SCREW  114204170\tMINI MAGNA-FX CANN SCREW  114205012\tMINI MAGNA-FX CANN SCREW  114205016\tMINI MAGNA-FX CANN SCREW  114205020\tMINI MAGNA-FX CANN SCREW  114205024\tMINI MAGNA-FX CANN SCREW  114205028\tMINI MAGNA-FX CANN SCREW  114205032\tMINI MAGNA-FX CANN SCREW  114205036\tMINI MAGNA-FX CANN SCREW  114205040\tMINI MAGNA-FX CANN SCREW  114205044\tMINI MAGNA-FX CANN SCREW  114205048\tMINI MAGNA-FX CANN SCREW  114205055\tMINI MAGNA-FX CANN SCREW  114205065\tMINI MAGNA-FX CANN SCREW  114205124\tMINI MAGNA-FX CANN SCREW  114205126\tMINI MAGNA-FX CANN SCREW  114205128\tMINI MAGNA-FX CANN SCREW  114205130\tMINI MAGNA-FX CANN SCREW  114205132\tMINI MAGNA-FX CANN SCREW  114205134\tMINI MAGNA-FX CANN SCREW  114205136\tMINI MAGNA-FX CANN SCREW  114205138\tMINI MAGNA-FX CANN SCREW  114205140\tMINI MAGNA-FX CANN SCREW  114205142\tMINI MAGNA-FX CANN SCREW  114205144\tMINI MAGNA-FX CANN SCREW  114205146\tMINI MAGNA-FX CANN SCREW  114205148\tMINI MAGNA-FX CANN SCREW  114205150\tMINI MAGNA-FX CANN SCREW  114205155\tMINI MAGNA-FX CANN SCREW  114205160\tMINI MAGNA-FX CANN SCREW  114205165\tMINI MAGNA-FX CANN SCREW  114205170\tMINI MAGNA-FX CANN SCREW    Product Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.",
      "product_quantity": "3190",
      "reason_for_recall": "As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013.  The affected products are sterile.",
      "recall_initiation_date": "20160111",
      "center_classification_date": "20160312",
      "termination_date": "20170413",
      "report_date": "20160323",
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      "more_code_info": ""
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}