{
  "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": "Ongoing",
      "city": "Gjovik",
      "state": "",
      "country": "Norway",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81977",
      "recalling_firm": "Moller Vital",
      "address_1": "Hadelandsvegen 2",
      "address_2": "P.o. Box 408",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution to Arizona, Delaware, Florida, Georgia, Massachusetts, Ohio, South Carolina, Texas, Washington, and Wisconsin.    Foreign distribution to Canada, Asia, Europe, and Australia.",
      "recall_number": "Z-1351-2019",
      "product_description": "Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016  1430017  1430021",
      "product_quantity": "427 total",
      "reason_for_recall": "The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.",
      "recall_initiation_date": "20190204",
      "center_classification_date": "20190516",
      "report_date": "20190522",
      "code_info": "All units manufactured between May 2013 and October 2018. Date of manufacture is labeled on the product.",
      "more_code_info": ""
    }
  ]
}