{
  "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": "Warsaw",
      "address_1": "2850 Frontier Dr",
      "reason_for_recall": "The device is a Left 8 hole plate but is incorrectly labeled and etched as a Right device.",
      "address_2": "",
      "product_quantity": "15 devices",
      "code_info": "Lot number: 7736703 and part number: 00-1050-4308",
      "center_classification_date": "20120720",
      "distribution_pattern": "Worldwide Distribution -- USA, including states of IN, GA, MI, FL, MO, OH, and SC and country of Australia.",
      "state": "IN",
      "product_description": "OrthoPediatrics PediLoc Locking Plate System, 4.5mm Contour Locking Compression Femur 8 Hole Plate Right.    Used for pediatric patients as indicated for pelvic, small and long bone fractures.",
      "report_date": "20120801",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "OrthoPediatrics Corp",
      "recall_number": "Z-2057-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "62351",
      "termination_date": "20130430",
      "more_code_info": "",
      "recall_initiation_date": "20120614",
      "postal_code": "46582-7001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}