{
  "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": "Miamisburg",
      "address_1": "452 Alexandersville Rd",
      "reason_for_recall": "One lot of instruments have etched on the Yoke of the Pedicle Screw a laser marking size of 7.5 x 55mm instead of 5.5 x 55mm as described on the product label.",
      "address_2": "",
      "product_quantity": "14 units",
      "code_info": "Lot #: 4084-01; M/N X073-5555; UDI: *+M697X07355551/$408401U*",
      "center_classification_date": "20150422",
      "distribution_pattern": "US Distribution to states of: KS, NV & TX.",
      "state": "OH",
      "product_description": "Xpress System Pedicle Screw Assembly, 5.5 x 55mm.   An internal fixation device for spinal surgery consisting of rods, pedicle screw assemblies (screw, cap, yoke) and cross bar connector assemblies.",
      "report_date": "20150429",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "X Spine Systems Inc",
      "recall_number": "Z-1512-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70774",
      "termination_date": "20151021",
      "more_code_info": "",
      "recall_initiation_date": "20150311",
      "postal_code": "45342-3658",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}