{
  "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": "Terminated",
      "city": "Malm¿",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68235",
      "recalling_firm": "Arjo Hospital Equipment AB",
      "address_1": "HANS MICHELSENSGATAN 10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1247-2015",
      "product_description": "Pressure IQ Evolve Mattress; Non-powered mattress replacement system.    Intended for patients with medium to high risk for developing pressure ulcers while on a mattress.",
      "product_quantity": "1,034 units",
      "reason_for_recall": "The firm received complaints regarding multiple mattresses were showing failures resulting in pressure ulcers.",
      "recall_initiation_date": "20140901",
      "center_classification_date": "20150306",
      "termination_date": "20160104",
      "report_date": "20150318",
      "code_info": "All Pressure IQ Evolve mattresses equipped with the 60g pods, manufactured January 2012-December 2013."
    }
  ]
}