{
  "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": "285",
      "code_info": "lot no.:  61771007  61827364  61853067  61865449  61870424  61888695  61953208  62230187  61853068  61870425  61953213  62230188  61860667  61895085  61937602  61953221  62230190  62271893  61900049  61900056  61958816  62124265  62124266  62241683  62255907  61778898  61860656  61870426  61853070  61900064  370958  61777470  61834885  61934150  370957  61888707  62271892",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 31 consists of all product under  product code: KTT and same usage:  Item no:\t  118113003\tFREE-LOCK TUBE & SCP PLAT  118113502\tFREE-LOCK TUBE & SCP PLAT  118113503\tFREE-LOCK TUBE & SCP PLAT  118114002\tFREE-LOCK TUBE & SCP PLAT  118114003\tFREE-LOCK TUBE & SCP PLAT  118114502\tFREE-LOCK TUBE & SCP PLAT  118114503\tFREE-LOCK TUBE & SCP PLAT  118115002\tFREE-LOCK TUBE & SCP PLAT  118115003\tFREE-LOCK TUBE & SCP PLAT    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-1129-2016",
      "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"
    }
  ]
}