{
  "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": "0",
      "code_info": "lot no.:  61902234  61930449  62238240  61781914  61818112  61873640  61873641  61921821  61930453  62142331  62171289  61656184  61656185  61663560  61818114  61818116  61818118  61873642  61930459  61969224  61969225  62118686  62238244  62250669  62279154  62279156  61640868  61781919  61781920  61866144  61866145  61969228  62122251  62142308  62171295  62255624  62279159  61663622  61781922  61781927  61831643  61862302  61930474  62142311  62232636  62238251  62283223  62283223N  61663623  61781928  61866147  62092290  62155425  62031720",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 14 consists of all product under  product code HSB  , and same usage:  Item no:\t  225600230\tASIA ONE-PIECE LAG SCREW  225600232\tASIA ONE-PIECE LAG SCREW  225600235\tASIA ONE-PIECE LAG SCREW  225600237\tASIA ONE-PIECE LAG SCREW  225600240\tASIA ONE-PIECE LAG SCREW  225600242\tASIA ONE-PIECE LAG SCREW  225600245\tASIA ONE-PIECE LAG SCREW  225600227\tASIA ONE-PIECE LAG SCREW 70MM    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-1112-2016",
      "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"
    }
  ]
}