{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Maryland Heights",
      "address_1": "10888 Metro Ct",
      "reason_for_recall": "During internal cycle testing of A-Series lifts Handicare has found that the A-Series lift strap for lifts manufactured between April 25, 2017 and June 12, 2017 may wear prematurely at max load (625 lbs). We have identified the root cause as a supplied component that was not to specification. If the strap wears during use there is a potential risk for the person being supported by the lift to drop.",
      "address_2": "",
      "product_quantity": "8 units",
      "code_info": "A6M0001526, A6M0001527, A6M0001528, A6M0001529, A6M0001530, A6M0001485, A6M0001486, A6M0001498",
      "center_classification_date": "20171006",
      "distribution_pattern": "Us and Canada",
      "state": "MO",
      "product_description": "PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered",
      "report_date": "20171018",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Handicare Usa Inc",
      "recall_number": "Z-0013-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "78096",
      "termination_date": "20181217",
      "more_code_info": "",
      "recall_initiation_date": "20170908",
      "postal_code": "63043-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}