{
  "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": "345 E Main St",
      "reason_for_recall": "After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and instructions for use to provide additional instructions and patient conditions that may place excessive loading on the polyethylene insert.",
      "address_2": "",
      "product_quantity": "5305 distribution events",
      "code_info": "Part numbers 00-5850-013-95",
      "center_classification_date": "20140117",
      "distribution_pattern": "Worldwide Distribution.  USA nationwide and Germany, with  further distribution into EU countries.",
      "state": "IN",
      "product_description": "Zimmer Segmental Systems; Polyethylene Inserts, Size C.    Knee replacement.",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-0784-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "66846",
      "termination_date": "20150224",
      "more_code_info": "",
      "recall_initiation_date": "20131219",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}