{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Laguna Hills",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91045",
      "recalling_firm": "Sonendo Inc",
      "address_1": "26051 Merit Cir Ste 104",
      "address_2": "N/A",
      "postal_code": "92653-7008",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - U.S. Nationwide distribution in the state of OH and the country of Canada.",
      "recall_number": "Z-0233-2023",
      "product_description": "GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02",
      "product_quantity": "15 instruments",
      "reason_for_recall": "Procedure Instruments with erroneous unit carton labels.",
      "recall_initiation_date": "20221014",
      "center_classification_date": "20221114",
      "report_date": "20221123",
      "code_info": "GentleWave System Anterior/Premolar Procedure Instrument (GW-APM-PI02) UDI-DI Code: 00858395006318 Lot Number: W2022080941R"
    }
  ]
}