{
  "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": "66536",
      "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": "Distributed in FL and MD.",
      "recall_number": "Z-0492-2014",
      "product_description": "Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7",
      "product_quantity": "24",
      "reason_for_recall": "The Columbus Revision CoCr 15 mm distal and posterior implant spacers, sizes F5-F7, were not compatible.",
      "recall_initiation_date": "20130919",
      "center_classification_date": "20131213",
      "termination_date": "20141222",
      "report_date": "20131225",
      "code_info": "lots: 51468773, 51447588, 51468302, 51503760, 51571394, 51585136, 51447597"
    }
  ]
}