{
  "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": "Charleston",
      "address_1": "415 Jessen Ln",
      "reason_for_recall": "Possible fatigue failure of the plastic joint may occur after an average use of seven years.",
      "address_2": "",
      "product_quantity": "287",
      "code_info": "Unknown",
      "center_classification_date": "20131212",
      "distribution_pattern": "US Distribution including the states of AR, CA, CO, KS, MA, MI, MO, NJ, NY, NC, OH, OK, PA, SD, TX and WA.",
      "state": "SC",
      "product_description": "Helion S Exam Light or H300    The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.",
      "report_date": "20131218",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Trumpf Medical Systems, Inc.",
      "recall_number": "Z-0484-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66790",
      "termination_date": "20170306",
      "more_code_info": "",
      "recall_initiation_date": "20130219",
      "postal_code": "29492-7906",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}