{
  "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": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73298",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of SD, MO, NY, MI, PA, KY and TN and in the country of Argentina.",
      "recall_number": "Z-1046-2016",
      "product_description": "M/L Taper Hip Prosthesis (Item: 00-7711-012-20, Lot: 62937093",
      "product_quantity": "9 units",
      "reason_for_recall": "Zimmer Biomet initiated a lot-specific voluntary recall on 02/11/2016, of the M/L Taper Hip Prosthesis.  single manufacturing lot of Size 12.5, Extended Offset, M/L Taper hip stems was incorrectly etched. The device was etched as \u0018STD,\u0019 rather than \u0018EXT.\u0019 The product packaging is labeled correctly as \u001cExtended.  Offset,\u001d and the device is an extended offset stem.",
      "recall_initiation_date": "20160211",
      "center_classification_date": "20160304",
      "termination_date": "20161201",
      "report_date": "20160316",
      "code_info": "Item: 00-7711-012-20, Lot: 62937093"
    }
  ]
}