{
  "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": [
    {
      "status": "Terminated",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86649",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "address_2": "PO Box 610",
      "postal_code": "18034-0610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution.    Model Name        ------------   Quantity distributed in U.S.    GF-UC140P-AL5  ------------- 1,297 devices  GF-UCT150-AL5  -------------  564 devices  GF-UCT180 --------------------  3,145 devices  GF-UM20 -----------------------     31 devices  GF-UM130 ---------------------     27 devices  GF-UMQ130 -------------------   373 devices  GF-UM160 ---------------------   299 devices  GF-UC160P-OL5 -------------    46 devices  GF-UCT160-OL5 -------------    49 devices  GF-UE160-AL5  -------------- 2,691 devices",
      "recall_number": "Z-0507-2021",
      "product_description": "Olympus Ultrasound Endoscope, Model number: GF-UE160-AL5 - Product Usage: used for endoscopic ultrasonic imaging of the gastrointestinal wall, bile and pancreatic ducts and surrounding organs.",
      "product_quantity": "2,691",
      "reason_for_recall": "A new inspection step was added to the cleaning and disinfection section of the Instructions For Use (IFU) for this device in order to reduce the risk of causing patient infections.",
      "recall_initiation_date": "20201016",
      "center_classification_date": "20201127",
      "termination_date": "20220607",
      "report_date": "20201209",
      "code_info": "All Serial/Lot Numbers",
      "more_code_info": ""
    }
  ]
}