{
  "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": [
    {
      "status": "Terminated",
      "city": "Mcmurray",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65823",
      "recalling_firm": "Stelkast Co",
      "address_1": "200 Hidden Valley Rd",
      "address_2": "N/A",
      "postal_code": "15317-2659",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide Distribution including TX, VA, OK,  and PA",
      "recall_number": "Z-2136-2013",
      "product_description": "SC2316, Distal Femoral Augment with Screw    Total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis and/or post-traumatic degenerative problems and revision of failed previous reconstructions.",
      "product_quantity": "11",
      "reason_for_recall": "The firm became aware of an incident relating to a breach of sterility in the sterility barrier packaging of SC2316, Distal Femoral Augment with Screw.",
      "recall_initiation_date": "20130624",
      "center_classification_date": "20130903",
      "termination_date": "20141008",
      "report_date": "20130911",
      "code_info": "Part number SC2316-3-5 with lot number 22389-111609. Part number SC2316-4-5 with lot number 22587-111609.  Part number SC2316-5-5 with lot number 23214-111609.",
      "more_code_info": ""
    }
  ]
}