{
  "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": {
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    }
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  "results": [
    {
      "status": "Ongoing",
      "city": "Pittsburgh",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93046",
      "recalling_firm": "Blue Belt Technologies, Inc",
      "address_1": "2875 Railroad St",
      "address_2": "N/A",
      "postal_code": "15201",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0041-2024",
      "product_description": "Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5)  Product Number: ROB10299",
      "product_quantity": "56 units",
      "reason_for_recall": "CORI software was missing a planning stage that appears in cases of significant knee deformation (outside of the range of 3 degrees valgus to 7 degrees varus) when the surgeon chooses to define the femoral rotational reference via the posterior condylar axis",
      "recall_initiation_date": "20230907",
      "center_classification_date": "20231005",
      "report_date": "20231011",
      "code_info": "UDI: (01) 00885556773338 Lot Numbers: 51141585, 51108475, 51108689"
    }
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}