{
  "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": "154",
      "code_info": "lot no.61951256  62230459  61907760  61907764  61926199  62261661  61926201  61907767  61907769  61907771  61909381  62230462  61907772  61196133  61907773  62020888  61920808",
      "center_classification_date": "20160312",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PR",
      "product_description": "Product 4 consists of all products under  product code HWC, and same usage:  Item no:\t  47482002603\t2.0 X 26 CORT SCREW CRUCI  47482002803\t2.0 X 28 CORT SCREW CRUCI  47482003203\t2.0 X 32 CORT SCREW CRUCI  47482003403\t2.0 X 34 CORT SCREW CRUCI  47482003603\t2.0 X 36 CORT SCREW CRUCI  47482003803\t2.0 X 38 CORT SCREW CRUCI  47482004003\t2.0 X 40 CORT SCREW CRUCI  47482004203\t2.0 X 42 CORT SCREW CRUCI  47482004403\t2.0 X 44 CORT SCREW CRUCI  47482004603\t2.0 X 46 CORT SCREW CRUCI  47482004803\t2.0 X 48 CORT SCREW CRUCI  47482005003\t2.0 X 50 CORT SCREW CRUCI  47482702000\t2.7 X 20 CORT SCREW HEX    \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \t  \tProduct Usage:  A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted 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-1102-2016",
      "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"
    }
  ]
}