{
  "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": "Portage",
      "address_1": "4100 E Milham Ave",
      "reason_for_recall": "Stryker Instruments initiated a voluntary recall of specific lots of Round Fluted Burs, due to tarnishing or corrosion which may be present on the recalled burs and could result in a foreign body reaction (inflammation) necessitating surgical intervention.",
      "address_2": "",
      "product_quantity": "25",
      "code_info": "5190-010-060 \u0013 Lot Numbers 15231017, 16033017, 16066017",
      "center_classification_date": "20160714",
      "distribution_pattern": "US Distribution to the states of : CA, IL, SD  Foreign: Canada, Netherlands",
      "state": "MI",
      "product_description": "6.0mm Round Fluted Bur, Super Long",
      "report_date": "20160720",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "recall_number": "Z-2205-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74562",
      "termination_date": "20170606",
      "more_code_info": "",
      "recall_initiation_date": "20160616",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}