{
  "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": "2026-04-22",
    "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": "77113",
      "recalling_firm": "Zimmer Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "No US distribution.  JAPAN  NETHERLANDS  SINGAPORE  SWITZERLAND",
      "recall_number": "Z-2059-2017",
      "product_description": "Bone Dowell Harvest Tubes",
      "product_quantity": "49",
      "reason_for_recall": "mislabeled as 8mm tube but it is  actually 9 mm in size. A 9mm subcomponent was erroneously substituted and etched as 8mm for the actual  8mm subcomponent part.",
      "recall_initiation_date": "20170412",
      "center_classification_date": "20170510",
      "termination_date": "20171103",
      "report_date": "20170517",
      "code_info": "Part Number: 900738  Lot Number (LN): 889990"
    }
  ]
}