{
  "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": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece.",
      "address_2": "",
      "product_quantity": "14",
      "code_info": "Hi-Line XXS handpiece;  Part Number - GB790R , Lot Number  4504385018  4504300008  4504328565  4504685847  4804685865",
      "center_classification_date": "20140103",
      "distribution_pattern": "Worldwide Distribution - USA including TX, NY, PA, and TN.  Internationally to Austria, Switzerland, Germany, Denmark, Spain, Finland, France, Hong Kong, Israel, Italy, Japan, Netherlands, Poland, Russian Federation, and Taiwan.",
      "state": "PA",
      "product_description": "Aesculap Hi-Line XXS handpiece    Hi-Line XXS handpieces are used with the HiLAN¿ and microspeed motor systems to hold burrs which cut and shape bone.",
      "report_date": "20140115",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aesculap, Inc.",
      "recall_number": "Z-0623-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67050",
      "termination_date": "20141202",
      "more_code_info": "",
      "recall_initiation_date": "20131209",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}