{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Aurora",
      "state": "NE",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98396",
      "recalling_firm": "Penner Patient Care, Inc.",
      "address_1": "101 Grant St",
      "address_2": "N/A",
      "postal_code": "68818-3200",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1501-2026",
      "product_description": "Penner Pacific Bathing Spa, Model Numbers 360020-1EP",
      "product_quantity": "10 units",
      "reason_for_recall": "The device does not bear a unique device identifier.",
      "recall_initiation_date": "20250813",
      "center_classification_date": "20260309",
      "report_date": "20260318",
      "code_info": "UDI-DI: 0085007365402; Serial Numbers: 03203147501 01192957001 06203171301 07203175701 11162597701 11193074801 11193074802 09193074801 09193074802 09193074803"
    }
  ]
}