{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "Two lots of hip implants are  mislabeled.",
      "address_2": "",
      "product_quantity": "24",
      "code_info": "Part Numbers: 1. 00-7864-013-00, Lot: 63703649; 2. 00-7864-013-20, Lot: 63703681",
      "center_classification_date": "20180309",
      "distribution_pattern": "Distributed in 2  US states: LA and NY. Distributed in Canada, China, Japan, and Switzerland.",
      "state": "IN",
      "product_description": "Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17) 250731 (10) 63703681)",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0939-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79397",
      "termination_date": "20190411",
      "more_code_info": "",
      "recall_initiation_date": "20180103",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}