{
  "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": [
    {
      "country": "United States",
      "city": "Mercedita",
      "address_1": "Turpeaux Industrial Park Rd 1 km 123.4",
      "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.",
      "address_2": "",
      "product_quantity": "37",
      "code_info": "lot no.:  61983647  62296609  62152979  62056816  61771916  61932061  61771919  62056817  61771920  61866489  61880386  61859716  61906564  62056818  61866490  61880387  61880388  61895979  61895980",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 24 consists of all product under  product code: HRS and same usage:  Item no:\t  234703104\tDISTAL MEDIAL FEMORAL CON  234703206\tDISTAL MEDIAL FEMORAL CON  234703208\tDISTAL MEDIAL FEMORAL CON  234800504\tDISTAL POSTERIOR/LATERAL  234800506\tDISTAL POSTERIOR/LATERAL  234800508\tDISTAL POSTERIOR/LATERAL  234800510\tDISTAL POSTERIOR/LATERAL  234800604\tDISTAL POSTERIOR/LATERAL  234800606\tDISTAL POSTERIOR/LATERAL  234800608\tDISTAL POSTERIOR/LATERAL  234800610\tDISTAL POSTERIOR/LATERAL  234800614\tDISTAL POSTERIOR/LATERAL    Product Usage:  Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1122-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "72900",
      "termination_date": "20170413",
      "more_code_info": "",
      "recall_initiation_date": "20160111",
      "postal_code": "00715",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}