{
  "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": "2026-08-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kaohsiung",
      "state": "",
      "country": "Taiwan",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99026",
      "recalling_firm": "United Orthopedic Corp.",
      "address_1": "No. 16 Luke 1st Rd.",
      "address_2": "Luzhu Dist.",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of Texas and Michigan.",
      "recall_number": "Z-2885-2026",
      "product_description": "Brand Name: U2 Total Knee System  Product Name: Femoral valgus adaptor, left and right  Model/Catalog Number: 9323-5333 and 9323-5334  Software Version: N/A  Product Description: Manual Orthopedic Surgical Instrument  Component: No",
      "product_quantity": "2",
      "reason_for_recall": "Due to an incomplete process of the component screw by a subcontractor which prevents the properly assembling of stem trail.",
      "recall_initiation_date": "20260520",
      "center_classification_date": "20260805",
      "report_date": "20260812",
      "code_info": "Product Number; UDI-DI Code; Lot Code: Product number 9323-5333; UDI-DI 04719886908084; Lot number 25FB50 Product number 9323-5334; UDI-DI 04719886908091; Lot number 25FB51",
      "more_code_info": ""
    }
  ]
}