{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.",
      "address_2": "",
      "product_quantity": "8",
      "code_info": "Item #110024464  Lot# 478340",
      "center_classification_date": "20180215",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "IN",
      "product_description": "G7 DUAL MOBILITY LINER 44MM F    Product Usage:  Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function and mobility to the damaged joint.",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0626-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79104",
      "termination_date": "20180816",
      "more_code_info": "",
      "recall_initiation_date": "20170825",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}