{
  "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": "2026-08-22",
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      "event_date_initiated": "2004-09-24",
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      "recall_status": "Terminated",
      "event_date_terminated": "2007-06-20",
      "res_event_number": "31193",
      "product_code": "FNG",
      "product_description": "UNO 102 EM/EE/ES Patient Lift",
      "code_info": "Serial Numbers: Range 33590-42291",
      "firm_fei_number": "3001451524",
      "recalling_firm": "Liko, Inc.",
      "address_1": "842 Upper Union St., Suite 4 842 Upper Union St.",
      "address_2": "Suite 4",
      "city": "Franklin",
      "state": "MA",
      "postal_code": "02038",
      "additional_info_contact": "Jim Butler\n888-545-6671",
      "reason_for_recall": "Incorrect length support screws may cause patient lift failure",
      "root_cause_description": "Other",
      "action": "Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.",
      "product_quantity": "21 units",
      "distribution_pattern": "Canada",
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