{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "Cleaning process validation failure.",
      "address_2": "",
      "product_quantity": "138 units",
      "code_info": "Part Number 42-5320-079-02   Lot Number 62613813  Part Number 42-5320-071-02   Lot Number 62625781  Part Number 42-5320-075-01   Lot Number 62619031  Part Number 42-5320-075-01   Lot Number 62619040  Part Number 42-5320-079-01   Lot Number 62626696  Part Number 42-5320-071-01   Lot Number 62625790",
      "center_classification_date": "20141108",
      "distribution_pattern": "US Nationwide Distribution and countries of Austria ,Belgium, Switzerland, Germany, France, United Kingdom, Italy and South Africa.",
      "state": "IN",
      "product_description": "Persona Stemmed 5 Degree Cemented Tibia      Product Usage:  This device is indicated for patients with severe knee pain and disability due to: \u001c Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis. \u001c Collagen disorders, and/or avascular necrosis of the femoral condyle. \u001c Post-traumatic loss of joint configuration, particularly when there is patellofemoral erosion, dysfunction or prior patellectomy. \u001c Moderate valgus, varus, or flexion deformities. \u001c The salvage of previously failed surgical attempts or for a knee in which satisfactory stability in flexion cannot be obtained at the time of surgery. \u001c This device is intended for cemented use only.",
      "report_date": "20141119",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-0198-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69397",
      "termination_date": "20150624",
      "more_code_info": "",
      "recall_initiation_date": "20141009",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}