{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cuyahoga Falls",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86694",
      "recalling_firm": "Coltene Whaledent Inc",
      "address_1": "235 Ascot Pkwy",
      "address_2": "N/A",
      "postal_code": "44223-3701",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Sold to distributors located in FL, NV, PA, TN, TX. Foreign distribution to Canada.",
      "recall_number": "Z-0468-2021",
      "product_description": "Strauss 25 Carbide  Dental Burs  (100057XXV)",
      "product_quantity": "556",
      "reason_for_recall": "The FG 557 bur was incorrectly packaged as the FG 57 bur. The FG 557 burs will remove more material than the FG 57 burs.",
      "recall_initiation_date": "20201020",
      "center_classification_date": "20201117",
      "report_date": "20201125",
      "code_info": "J77147  J93636"
    }
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}