{
  "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": "Zimmer is initiating a voluntary recall of specific identified lots due to the potential that the threads may be out of specification.",
      "address_2": "",
      "product_quantity": "41,180 total",
      "code_info": "Size 8, includes the following Lot numbers:  370321  37213648  37216196  61424999  61543980  62029931  62390069",
      "center_classification_date": "20140627",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Australia, China, Hong Kong, India, Japan, Korea, Malaysia, Nicaragua, Singapore, and Taiwan.",
      "state": "IN",
      "product_description": "NexGen Complete Knee Solution, MIS Total Knee Procedure, Stemmed Tibial Component, Precoat, Fixed Bearing, Size 8.     Part of the NexGen systems of semi-constrained, non-linked condylar knee prosthesis.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1939-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68457",
      "termination_date": "20151029",
      "more_code_info": "",
      "recall_initiation_date": "20140519",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}