{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kent",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94207",
      "recalling_firm": "Emergency Products & Research",
      "address_1": "890 W Main St",
      "address_2": "N/A",
      "postal_code": "44240-2284",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA, MI, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA.",
      "recall_number": "Z-1395-2024",
      "product_description": "O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.",
      "product_quantity": "190,000 units",
      "reason_for_recall": "Failure of adhesive to secure the pole insert.",
      "recall_initiation_date": "20240227",
      "center_classification_date": "20240328",
      "report_date": "20240403",
      "code_info": "Model EP-800; Lot No. 20230523-04, 09082023-11, 09082023-12, 122023-3, 122023-2, 122023-1.",
      "more_code_info": ""
    }
  ]
}