{
  "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": "56 E Bell Dr",
      "reason_for_recall": "It was identified that the product was not assembled correctly causing the implant shaft to shift and fall out during the opening of the device, which potentially could break the device.",
      "address_2": "",
      "product_quantity": "429 units",
      "code_info": "Item # 110019010  Lot #'s  017350 141990 142000 142020 167190 240720 240740 240770 257970 398710  398730 398740 398750 421780 421790 421800 465910 504120 813190 940370",
      "center_classification_date": "20180314",
      "distribution_pattern": "TX, NC, FL, PA, IN, WI, VA, NY, NJ, AL, CT",
      "state": "IN",
      "product_description": "fastener, fixation, nondegradable, soft tissue",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1009-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79273",
      "termination_date": "20200512",
      "more_code_info": "",
      "recall_initiation_date": "20171025",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}