{
  "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": "Lulea",
      "state": "N/A",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80911",
      "recalling_firm": "Liko AB",
      "address_1": "Alvik 7555",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "The products were distributed to the following US states: OH.",
      "recall_number": "Z-0105-2019",
      "product_description": "Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.",
      "product_quantity": "2",
      "reason_for_recall": "The products manufactured on 5/5/17 may be assembled incorrectly.  If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.",
      "recall_initiation_date": "20180717",
      "center_classification_date": "20181012",
      "termination_date": "20190419",
      "report_date": "20181024",
      "code_info": "Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05."
    }
  ]
}