{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "One piece from a different lot mixed with lot 236840 and is incorrectly etched as -6MM offset instead of +3MM offset. As the incorrect etching and related size difference affects the functional use of this product, the affected lot is being removed from the field.",
      "address_2": "",
      "product_quantity": "23",
      "code_info": "11-363660 UDI Number: (01) 00880304210509 (17) 270507 (10) 236840    Product Number: 11-363660  Lot Number: 236840",
      "center_classification_date": "20180314",
      "distribution_pattern": "Outside USA",
      "state": "IN",
      "product_description": "36MM COCR MODULAR HD -6MM",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1008-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79254",
      "termination_date": "20180820",
      "more_code_info": "",
      "recall_initiation_date": "20170915",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}