{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Bartlett",
      "address_1": "2925 Appling Rd",
      "reason_for_recall": "\"Chattering\" when cutting burrs are used in bone.",
      "address_2": "",
      "product_quantity": "324",
      "code_info": "Catalog No. (UDI-DI): MBUR5060FRCV (00821925036529), MBUR6060FRCV (00821925036536), and MBUR7060FRCV (00821925036543) ALL LOTS MANUFACTURED BEFORE AUGUST 3, 2017",
      "center_classification_date": "20180410",
      "distribution_pattern": "NM, MI, and TX  EU, Australia, Japan, and Hong Kong",
      "state": "TN",
      "product_description": "Gyrus ACMI Round Cutting Burrs - to be used with the Diego Elite system",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Gyrus ACMI, Inc.",
      "recall_number": "Z-1337-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79548",
      "more_code_info": "",
      "recall_initiation_date": "20170803",
      "postal_code": "38133-3901",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}