{
  "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": "Maryland Heights",
      "address_1": "10888 Metro Ct",
      "reason_for_recall": "The black plastic puck on the carry bar is breaking resulting in potential for patient harm.",
      "address_2": "",
      "product_quantity": "not greater than 17,964 units",
      "code_info": "There are no lot numbers, serial numbers, or UPC codes, only the model numbers.    Model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.",
      "center_classification_date": "20161209",
      "distribution_pattern": "Distributed US nationwide and to Canada, Japan, Australia, Thailand, Great Britain, and South Korea",
      "state": "MO",
      "product_description": "Carry bar which is an accessory to a lift used for patients in hospitals and other facilities.  Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757.",
      "report_date": "20161221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "ErgoSafe Products, LLC (DBA) Prism Medical",
      "recall_number": "Z-0728-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74488",
      "termination_date": "20180718",
      "more_code_info": "",
      "recall_initiation_date": "20160830",
      "postal_code": "63043-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}