{
  "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": "Corona",
      "address_1": "252 Mariah Cir",
      "reason_for_recall": "The Panacea Air Pro Mattress Control Unit is being recalled due to a firmware problem, which may result in the device not having the firmness range required.",
      "address_2": "",
      "product_quantity": "31 units",
      "code_info": "Serial No. 9500051 sequential to 9500300.",
      "center_classification_date": "20160819",
      "distribution_pattern": "Distributed to the US -- WI, OH, IL, TX, AZ, MD, IA, PA, CO, WA, ID, MN, LA, WY, and MS.",
      "state": "CA",
      "product_description": "Panacea Air Pro Mattress Control Unit, Model: Platinum 5000, US Model Number 5000.    Use with alternating pressure air flotation mattress.",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "American National Mfg Inc",
      "recall_number": "Z-2605-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74737",
      "termination_date": "20170117",
      "more_code_info": "",
      "recall_initiation_date": "20160711",
      "postal_code": "92879-1751",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}