{
  "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": "58320",
      "code_info": "lot no.:  62133636  61882374  61964347  61987304  62133643  62171285  62298481  61969229  62080367  62292385  61657722  61930479  61930480  61930481  62109268  61136016  61930482  62098917  62098918  61764507  61764508  61764509  61895897  61895905  61895907  61895908",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 55 consists of all product under product code: HSB and same usage:  Item no:\t  225900132\tONE-PIECE LAG SCREW 11MM  225900135\tONE-PIECE LAG SCREW 11MM  225900137\tONE-PIECE LAG SCREW 11MM  225900140\tONE-PIECE LAG SCREW 11MM  225900142\tONE-PIECE LAG SCREW 11MM  225900145\tONE-PIECE LAG SCREW 11MM  225900152\tONE-PIECE LAG SCREW 11MM  Usage:  An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.",
      "report_date": "20160323",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Manufacturing B.V.",
      "recall_number": "Z-1153-2016",
      "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"
    }
  ]
}