{
  "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": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67795",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) in states of: US: GA, WI, NJ, CA, NY, NC, PA, FL, CT, ME, TX, and IL; and countries of: Australia and Canada.",
      "recall_number": "Z-1496-2014",
      "product_description": "TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell  with Cluster Holes, Porous 60mm.   Catalog number 00-6202-060-22; Hip implant component.",
      "product_quantity": "17 units",
      "reason_for_recall": "The shell was missing the locking ring.",
      "recall_initiation_date": "20140401",
      "center_classification_date": "20140424",
      "termination_date": "20140911",
      "report_date": "20140430",
      "code_info": "00-6202-060-22; lot 62490588",
      "more_code_info": ""
    }
  ]
}