{
  "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": "Pelham",
      "state": "AL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97480",
      "recalling_firm": "Folsom Metal Products, Inc.",
      "address_1": "1449 Court Pl",
      "address_2": "N/A",
      "postal_code": "35124-1858",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, CA, FL, GA, IL, MD, MI, PA, TX.",
      "recall_number": "Z-2581-2025",
      "product_description": "Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile",
      "product_quantity": "490 units",
      "reason_for_recall": "Labeling includes shelf life that has not been validated.",
      "recall_initiation_date": "20250821",
      "center_classification_date": "20250917",
      "report_date": "20250924",
      "code_info": "All lots distributed from August 1, 2020, to July 30, 2025/UDI:00850014548056"
    }
  ]
}