{
  "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": [
    {
      "status": "Completed",
      "city": "Katikati",
      "state": "",
      "country": "New Zealand",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84126",
      "recalling_firm": "RHONDIUM LIMITED",
      "address_1": "4 Sheffield Street",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution was made to IL, NM, TX, and WI.  There was no foreign/military/government distribution.",
      "recall_number": "Z-0708-2020",
      "product_description": "Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx.  The firm name on the label is Rhondium Ltd., Katikati, New Zealand.",
      "product_quantity": "6 devices",
      "reason_for_recall": "The product was mislabeled with an incorrect expiration date.",
      "recall_initiation_date": "20190131",
      "center_classification_date": "20191219",
      "report_date": "20191225",
      "code_info": "Lot numbers 1832-1099 and 1828-0982.",
      "more_code_info": ""
    }
  ]
}