{
  "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": [
    {
      "status": "Terminated",
      "city": "Gjovik",
      "state": "N/A",
      "country": "Norway",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64512",
      "recalling_firm": "Moller Vital",
      "address_1": "Hadelandsvegan 2,",
      "address_2": "P.o. Box 408",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide Distribution:  CA, FL, GA, ID, IL, KY, MA, ME, MI, MN, NC, NH, NJ, NM, NV, NY, OH, OK, PA, TN, TX, VT, WA and Hawaii.    Foreign Distribution:: Australia, Austria; Belgium, Denmark, Finland, France, Germany, Iceland, Israel, Italy, Japan, Netherlands, New Zealand, Norway, Spain, Sverige, Switzerland, United Kingdom.",
      "recall_number": "Z-1343-2013",
      "product_description": "Molift Smart 150",
      "product_quantity": "Subject to recall 1,460 units; US: 175 units; Foreign: 1,285 units",
      "reason_for_recall": "The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.",
      "recall_initiation_date": "20130215",
      "center_classification_date": "20130521",
      "termination_date": "20140711",
      "report_date": "20130529",
      "code_info": "Art #: 0920008;  Serial Number range 20941 to 27299."
    }
  ]
}