{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63223",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Within the US, product was distributed to PA and TN.",
      "recall_number": "Z-0082-2013",
      "product_description": "Columbus 4-IN-1 Femoral Cutting Guide M3 Instrument (NQ083R)",
      "product_quantity": "2",
      "reason_for_recall": "The manufacturer informed the recalling firm of a potential laser marking error in size identification on two Columbus 4-IN-1 Femoral Cutting Guide Instruments.  The guides are correctly dimensioned, but the laser markings have been incorrectly etched.",
      "recall_initiation_date": "20120509",
      "center_classification_date": "20121018",
      "termination_date": "20140115",
      "report_date": "20121024",
      "code_info": "NQ083R"
    }
  ]
}