{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lewisville",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99225",
      "recalling_firm": "Orthofix U.S. LLC",
      "address_1": "3451 Plano Pkwy",
      "address_2": "",
      "postal_code": "75056-9453",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US: AZ\tCA\tCO\tCT\tFL\tGA\tID\tIL\tIN\tLA\tMD\tMI\tMO\tMS\tMT\tNC\tNY\tOH\tOR\tSC\tSD\tTX\tUT\tVA\tWA\tWI\t  OUS: None",
      "recall_number": "Z-2732-2026",
      "product_description": "Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS  REF: M122, Unilateral orthopedic/trauma external fixation device",
      "product_quantity": "62 units",
      "reason_for_recall": "Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111",
      "recall_initiation_date": "20260610",
      "center_classification_date": "20260714",
      "report_date": "20260722",
      "code_info": "All Lots; GTIN# 18032568866711",
      "more_code_info": ""
    }
  ]
}