{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Center Valley",
      "address_1": "3500 Corporate Pkwy",
      "reason_for_recall": "The adhesive used in the repair of the endoscope was incorrectly prepared.  It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.",
      "address_2": "PO Box 610",
      "product_quantity": "1",
      "code_info": "Serial Number 7621683",
      "center_classification_date": "20190312",
      "distribution_pattern": "US Nationwide distribution in the states of  CT, IL, MN, MO, and NC.",
      "state": "PA",
      "product_description": "Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.",
      "report_date": "20190320",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Olympus Corporation of the Americas",
      "recall_number": "Z-1007-2019",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "82099",
      "termination_date": "20201118",
      "recall_initiation_date": "20181217",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}