{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Magog",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92175",
      "recalling_firm": "Arjohuntleigh Magog, Inc.",
      "address_1": "2001 Tanguay St",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  OH, NY",
      "recall_number": "Z-1629-2023",
      "product_description": "Arjo Portable Scale Adaptor, Model Number 700.05725; accessory intended to be used in combination with compatible patient lifting equipment",
      "product_quantity": "3",
      "reason_for_recall": "Some Arjo Portable Scale Adaptors have been assembled with straps that have a potential to detach.",
      "recall_initiation_date": "20230217",
      "center_classification_date": "20230524",
      "report_date": "20230531",
      "code_info": "UDI/DI 05055982760713, Serial Numbers:  300501841, 300501842, 300515661"
    }
  ]
}