{
  "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": "119",
      "code_info": "lot no.:  61895477  62274946  61771936  61859733  61895479  62049380  62274957  62274957N  61879883  61771950  61879872  61879874  61918348  61944990  62199039  62312399  62312401  62312402  62312401N  61859738  61944992  62124572  62124572N  61941119  62296602  62233795  62312404  62312404N  61944994  62134044  61771903  62152982  61941121  61944995  62233794  62233796  62296608  61771908  62180987",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 58 consists of all product under product code: HRS and same usage:  Item no:\t  234800904\tPROXIMAL DORSAL ULNA PLT  234800906\tPROXIMAL DORSAL ULNA PLT  234800908\tPROXIMAL DORSAL ULNA PLT  234800910\tPROXIMAL DORSAL ULNA PLT  234801004\tPROXIMAL DORSAL ULNA PLT  234801006\tPROXIMAL DORSAL ULNA PLT  234801008\tPROXIMAL DORSAL ULNA PLT  234801010\tPROXIMAL DORSAL ULNA PLT 10H LT  234701304\tPROXIMAL MEDIAL TIBIAL 4.  234701306\tPROXIMAL MEDIAL TIBIAL 4.  234701308\tPROXIMAL MEDIAL TIBIAL 4.  234701404\tPROXIMAL MEDIAL TIBIAL 4.  234701406\tPROXIMAL MEDIAL TIBIAL 4.  234701408\tPROXIMAL MEDIAL TIBIAL 4.    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-1156-2016",
      "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"
    }
  ]
}