{
  "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": "4752",
      "code_info": "lot no.:  61793328  62253390  61641813  62194666  61993625  62262085  62313056  62313056N  62021140  62312364  62312364N  61817404  61809837  61851878  61987145  62165485  62244841  62244854  61763549  61826386  61851889  61968098  62114111  62114112  62172486  61804389  61841502  61872521  61962448  61983689  62137121  62244852  61665045  61841504  62031683  62137150  62244853  61809838  62306323  62306323N  61830462  61809839  62189554  61804722  61830471  62165499  62165501  62189558  61809843",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 38 consists of all product under  product code: HSB and same usage:  Item no:\t  225303255\tINTERLOCKING IM SCREW LG  225303555\tINTERLOCKING IM SCREW LG  225303755\tINTERLOCKING IM SCREW LG  225307055\tINTERLOCKING IM SCREW LG  225302742\tINTERLOCKING IM SCREW MED  225303242\tINTERLOCKING IM SCREW MED  225307042\tINTERLOCKING IM SCREW MED  225302737\tINTERLOCKING IM SCREW SML  225303237\tINTERLOCKING IM SCREW SML    Product 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-1136-2016",
      "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"
    }
  ]
}