{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mcmurray",
      "address_1": "200 Hidden Valley Rd",
      "reason_for_recall": "Firm was made aware of incidents relating to the difficulty of properly engaging and securing the Cross-Over 36mm liner into the Cross-Over shell.",
      "address_2": "",
      "product_quantity": "254",
      "code_info": "Part Numbers SC3458-52, lot number 28820-112612; SC3474-52, lot number 28822-101812; SC3459-52, lot number 28823-101812; and SC3460-52, lot number 28821-000.",
      "center_classification_date": "20130406",
      "distribution_pattern": "Nationwide Distribution including the states of NV, OK and PA.",
      "state": "PA",
      "product_description": "Stelkast Cross-over Acetabular Shell and Liner Hip System, Part Numbers SC3458-52, SC3474-52, SC3459-52, and SC3460-52.    Intended for use in reconstruction of the articulating surface of the acetabular portion of the hip.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stelkast Co",
      "recall_number": "Z-1066-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "64505",
      "termination_date": "20141008",
      "more_code_info": "",
      "recall_initiation_date": "20130124",
      "postal_code": "15317-2659",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}