{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "345 E Main St",
      "reason_for_recall": "Based on a review of historic packaging validations, it was determined that a subset of product packaged at a Zimmer facility required testing to ensure that previously packaged product from this facility met the established requirements for sterile barrier integrity.  This testing determined that a packaging tray configuration which consists of an inner and outer sterile tray, resulted in failure",
      "address_2": "",
      "product_quantity": "42, 065 units total",
      "code_info": "Item #'s:   00-2347-001-12  00-2347-001-14  00-2347-001-16  00-2347-001-18  Lot #s:  All lots with an expiration date prior to July 24, 2023",
      "center_classification_date": "20131227",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "IN",
      "product_description": "FEM COND BUTTRESS PLT, RT.",
      "report_date": "20140108",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-0585-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "66499",
      "termination_date": "20150505",
      "more_code_info": "",
      "recall_initiation_date": "20131105",
      "postal_code": "46580-2746",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}