{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85524",
      "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 and the countries of Canada, AHMADABAD, GUJARAT, BANGKOK, BELROSE NSW, BUENOS AIRES, CHILE, COSTA RICA, HIRATSUKA CITY,                        HUECHURABA SANTIAGO, INDIA, JAPAN, MEXICO DF, NETHERLANDS, PICHINCHA, EC, SAN JOSE,                             SINGAPORE, TAIWAN, THAILAND, YONGSAN-GU SEOUL.",
      "recall_number": "Z-2156-2020",
      "product_description": "Knee Products:  \t  TMJPM-1510 Microfixation\tCustom Made Device, Left PM-TMJ Model\t(01)00841036226534(17)220111(10)735550  Product Usage: Knee prosthesis",
      "product_quantity": "1",
      "reason_for_recall": "Potential presence of elevated endotoxin levels that exceed the specification limit",
      "recall_initiation_date": "20200417",
      "center_classification_date": "20200528",
      "termination_date": "20210625",
      "report_date": "20200603",
      "code_info": "Lot Number/UDI:  735550  (01)00841036226534(17)220111(10)735550"
    }
  ]
}