{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "112644",
      "product_res_number": "Z-0061-2013",
      "event_date_initiated": "2012-09-13",
      "event_date_posted": "2012-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-01-15",
      "res_event_number": "63124",
      "product_description": "CPT Hip System Femoral Stem Petite, Item No. 00-8011-000-05.\n\nCPT stems are primary cemented femoral hip stems used by surgeons in total hip arthroplasty.",
      "code_info": "Lot 62017554",
      "firm_fei_number": "1000220733",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "345 E Main St",
      "city": "Warsaw",
      "state": "IN",
      "postal_code": "46580-2746",
      "additional_info_contact": "Dawn Kindle\n574-372-4807",
      "reason_for_recall": "Zimmer Inc. is initiating a removal of the CPT Modular Stem (item 00-8011-001-00), CPT Stem Petite (item 00-8011-000-05; ) and CPT Femoral Stem 12/14 Neck Taper Extended Offset,(item 00-8114-001-10 ) because devices were packaged in incorrect cartons and distributed internationally and domestically.   Zimmer received five complaints of this packaging issue.",
      "root_cause_description": "Packaging change control",
      "action": "Zimmer Inc. sent an \"URGENT MEDICAL DEVICE RECALL-LOT SPECIFIC\" letter dated September 13, 2012 to all affected customers.  The letter identified the product, problem, and actions to be taken by the customers.  Consignees were asked to return all recalled product with a completed Inventory Return Certification Form.  Contact the firm at 1-800-348-2759 for questions regarding this notice.",
      "product_quantity": "20",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of Indiana and Oklahoma and the countries of Australia, Thailand, Malaysia, Germany, India, Bulgaria, Egypt, UK, Russian FED, Slovak, and Brazil.",
      "openfda": {}
    }
  ]
}