{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bridgend South Wales",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76179",
      "recalling_firm": "Biomet U.K., Ltd.",
      "address_1": "Waterton Industrial Estate",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution in the states of LA, NC, AR, MT, MO, CA, NY, KS, TX, MA, KY, OK, SC, NJ and the countries of Foreign: THAILAND, JAPAN, NETHERLANDS",
      "recall_number": "Z-1162-2017",
      "product_description": "Oxford Partial Knee System Right Medial Tibial Trial Tray Size D  Product Usage:  Instruments for use with the Oxford Uni Partial Knee System",
      "product_quantity": "72",
      "reason_for_recall": "Zimmer Biomet is conducting a medical device field action for various lot-specific Oxford Knee instruments due to potential alumina inclusions in the raw material batch used to produce the affected products. Inclusions contained within the finished product could lead to the cracking and separation of the instrument.",
      "recall_initiation_date": "20160105",
      "center_classification_date": "20170222",
      "termination_date": "20180630",
      "report_date": "20170301",
      "code_info": "Item: 32-420735, Lots: ZB160501, ZB160601, ZB160801"
    }
  ]
}