{
  "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": "Magog",
      "state": "Quebec",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81872",
      "recalling_firm": "Arjohuntleigh Magog",
      "address_1": "2001 Rue Tanguay",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "US, Saudi Arabia, and Kuwait",
      "recall_number": "Z-0802-2019",
      "product_description": "ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800",
      "product_quantity": "231 units",
      "reason_for_recall": "Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.",
      "recall_initiation_date": "20181219",
      "center_classification_date": "20190205",
      "termination_date": "20220126",
      "report_date": "20190213",
      "code_info": "All Serial Numbers",
      "more_code_info": ""
    }
  ]
}