{
  "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": "1800 W Center St",
      "reason_for_recall": "A complaint was received for Item 42-5320-067-02, lot 63236047. It was report that there was no set screw or taper plug included in the box. Complaint investigation confirmed that the entire lot of 63236047 was missing the set screw and taper plug.",
      "address_2": "",
      "product_quantity": "3 units",
      "code_info": "Item# 42-5320-067-02  Lot # 63236047",
      "center_classification_date": "20180327",
      "distribution_pattern": "Non-USA Customer",
      "state": "IN",
      "product_description": "PERSONA¿ THE PERSONALIZED KNEE SYSTEM \"PSN TIB STM 5 DEG SZ D R\" indicated for patients with severe knee pain and disability due to: - Rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis.",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1224-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79394",
      "termination_date": "20190409",
      "more_code_info": "",
      "recall_initiation_date": "20171212",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}