{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Draper",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85157",
      "recalling_firm": "Ortho Development Corporation",
      "address_1": "12187 S Business Park Dr",
      "address_2": "N/A",
      "postal_code": "84020-8663",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US: CA, FL, OH, PA, TX, and UT.  OUS: Japan.",
      "recall_number": "Z-1903-2020",
      "product_description": "Tibial Tray Nonporous A Size 2; Model # PN 162-1200-A; Material: Ti6Al4V.",
      "product_quantity": "27",
      "reason_for_recall": "The locking mechanism of  the tibial tray exhibited a  manufacturing defect in which a uniform ridge was cut along the inner wall of  the  \"T\"  and  \"Y\" junctions, which may cause resistance when the Tibial Insert was being assembled.",
      "recall_initiation_date": "20190530",
      "center_classification_date": "20200505",
      "report_date": "20200513",
      "code_info": "Lot Number: A200590",
      "more_code_info": ""
    }
  ]
}