{
  "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": "West Chester",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66414",
      "recalling_firm": "Synthes USA HQ, Inc.",
      "address_1": "1302 Wrights Ln E",
      "address_2": "N/A",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including IN, MT, HI, and FL.",
      "recall_number": "Z-0410-2014",
      "product_description": "Vertebroplasty Needle Kit 10g Diamond Tip     Intended to be used to inject PMMA cement into vertebral bodies during Vertebroplasty procedure.",
      "product_quantity": "40",
      "reason_for_recall": "Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplasty Needle Kit 10g Diamond Tip device.",
      "recall_initiation_date": "20130730",
      "center_classification_date": "20131126",
      "termination_date": "20150416",
      "report_date": "20131204",
      "code_info": "Part No. 03.702.218S, Lot No. AJM838X"
    }
  ]
}