{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94405",
      "recalling_firm": "Wishbone Medical, Inc.",
      "address_1": "100 Capital Dr",
      "address_2": "N/A",
      "postal_code": "46582-6704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution to Florida, New Jersey and Connecticut.",
      "recall_number": "Z-1808-2024",
      "product_description": "WishFIX Growth Control Plating System, Model Number: TEFCS28-080US. Orthopedic device.",
      "product_quantity": "60 units",
      "reason_for_recall": "The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated.",
      "recall_initiation_date": "20240405",
      "center_classification_date": "20240510",
      "report_date": "20240522",
      "code_info": "Model Number: TEFCS28-08-US; UDI/DI: B562TEFCS2808US0; Lot Number: 28042"
    }
  ]
}