{
  "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": "2026-04-15",
    "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": "72646",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and country of: Canada.",
      "recall_number": "Z-0448-2016",
      "product_description": "Tray Set containing multiple instruments and may contain the flexible bone awl, flexible drill and/or flexible screw driver in varying amounts depending on order. Tray set is not sealed.      These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.     Tray catalog number is: Tray designated as ST0485-037.",
      "product_quantity": "unknown",
      "reason_for_recall": "The flexible shaft of the instruments may break during orthopedic spinal surgery.  There is a risk of a delay in surgery or that a fragment from the shaft could be left in a patient.",
      "recall_initiation_date": "20151110",
      "center_classification_date": "20151218",
      "termination_date": "20160908",
      "report_date": "20151230",
      "code_info": "All Lots"
    }
  ]
}