{
  "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": "62240",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution, including the states of CA, CO, IL, LA, NV, OH, and TX .",
      "recall_number": "Z-1934-2012",
      "product_description": "S4 Cervical (S4C) Revision Instruments (FW099R and FW101R).  The S4C Revision Instruments assist in the removal of an occipital cervical screw during revision surgery.",
      "product_quantity": "15",
      "reason_for_recall": "Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4 Cervical (S4C) Occiput Revision Instrument that is part of the S4C Occipital Instrument Set.  The instruments may not thread into the screw properly during a revision surgery due to tolerance issues between the two instruments.",
      "recall_initiation_date": "20120307",
      "center_classification_date": "20120703",
      "termination_date": "20120808",
      "report_date": "20120711",
      "code_info": "All distributed lot numbers and serial numbers"
    }
  ]
}