{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Biomet investigation identified that the square end of the offset tibial tray adaptor locking insert is oversized and may not engage insert tool screwdriver.   This could cause a possible delay in surgery greater than 30 minutes, potentially exposing the patient to the increased risks from being under anesthesia for a longer duration.",
      "address_2": "",
      "product_quantity": "200",
      "code_info": "Catalog Number:  141490  Lot 378330,378320,407230,485010,505140,485000,506070,533400,54048, 439700,797820",
      "center_classification_date": "20121217",
      "distribution_pattern": "Worldwide distribution - USA (nationwide) and the countries of Australia,  Canada, Chile, Europe, Japan,  Korea, Panama, Puerto Rico and Thailand.",
      "state": "IN",
      "product_description": "Biomet Offset Tibial Tray 2.5 mm Adaptor, REF 141490  Sterile, QTY.1    Product Usage:  Knee joint replacement prostheses intended for application with or without bone cement. Knee joint replacement components include femoral, tibial, and patellar components, intended for both primary and revision applications. Indications: 1) painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis when one or more compartments are involved, 2) correction of varus, valgus, or posttraumatic deformity, 3) correction or revision of unsuccessful osteotomy, arthrodesis, or failure of previous joint replacement procedure",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-0533-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63781",
      "termination_date": "20131108",
      "more_code_info": "",
      "recall_initiation_date": "20121115",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}