{
  "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": "Anyang",
      "state": "N/A",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79830",
      "recalling_firm": "IntroMedic Co., Ltd.",
      "address_1": "F-Rtek 6 Floor",
      "address_2": "11-25 Simindaero327beon-Gil; Dongan",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Us Nationwide Distribution in the states of:  NY, MD, TX, IL, IN, KY, FL, OH, TN, CA, GA, KS, MO & NC",
      "recall_number": "Z-1615-2018",
      "product_description": "Miriam Capsule Endoscope System. Model MR1100    Product Usage:  MiroCam Capsule Endoscope System is intended for visualization of the small bowel mucosa. It may be used as a tool in the detection of abnormalities of the small bowel in adults.",
      "product_quantity": "82",
      "reason_for_recall": "When a user switches on MR1100 Receiver, even though the battery was fully charged, the LED was displayed as orange color due to momentary drop of battery voltage.",
      "recall_initiation_date": "20170215",
      "center_classification_date": "20180503",
      "termination_date": "20180808",
      "report_date": "20180509",
      "code_info": "None"
    }
  ]
}