{
  "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": "2026-03-18",
    "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": "91365",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of IN, KY and the countries of Canada, New Zealand, Japan, Netherlands.",
      "recall_number": "Z-1018-2023",
      "product_description": "Oxford Partial Knee System, Fixed Lateral Tibial Construct- Intended to replace part of a knee joint when used in conjunction with a femoral and tibial component  Item Number: 154341",
      "product_quantity": "7 units",
      "reason_for_recall": "Packaged in the incorrect shelf carton.   Incorrect shelf carton; outer carton is smaller than the required outer carton, which forces the Tyvex pouch  to be folded and packaged in the carton causing compound creases and compromise the sterile barrier",
      "recall_initiation_date": "20221215",
      "center_classification_date": "20230126",
      "report_date": "20230201",
      "code_info": "UDI: (01) 05019279515349 (17) 241123 (10) 077830 Lot Number: 077830",
      "more_code_info": ""
    }
  ]
}