{
  "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": "West Chester",
      "address_1": "1302 Wrights Ln E",
      "reason_for_recall": "Two lots of the Synthes XRL Medium Trial-Central Body device were incorrectly etched with the incorrect dimensions for height.",
      "address_2": "",
      "product_quantity": "3",
      "code_info": "Product no. 03.807.507, lot no. 8029684, and product no. 03.807.508, lot no. 8029689.",
      "center_classification_date": "20140602",
      "distribution_pattern": "US Distribution including the states of FL, NJ and MN.",
      "state": "PA",
      "product_description": "Synthes XRL Medium Trial - Central Body, an instrument used as part of the Synthes XRL System, a vertebral body replacement device.   For spinal surgery. The Synthes XRL device is intended to be used with the Synthes supplemental internal fixation systems (e.g., USS, including MATRIX, Pangea, and TSLP).",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes, Inc.",
      "recall_number": "Z-1681-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68006",
      "termination_date": "20150910",
      "more_code_info": "",
      "recall_initiation_date": "20140408",
      "postal_code": "19380-3417",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}