{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "210677",
      "product_res_number": "Z-0351-2025",
      "event_date_initiated": "2024-09-13",
      "event_date_posted": "2024-11-08",
      "recall_status": "Open, Classified",
      "res_event_number": "95584",
      "product_code": "GCP",
      "k_numbers": [
        "K790071"
      ],
      "product_description": "Brand Name: Olympus\nProduct Name: Cystoscope Outer Sheath\nModel/Catalog Number: WA22810A\nSoftware Version: N/A\nProduct Description: Outer sheaths can be combined with rigid Telescopes.\nComponent: N/A",
      "code_info": "Model: WA2280A, UDI:  04042761051729, Lot#: All lots.",
      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-8229",
      "additional_info_contact": "Cynthia Ow\n647-9993203",
      "reason_for_recall": "Olympus is removing the statement of compatibility with a GreenLight Laser for BPH therapy from the Instruction for Use (IFU) due to the potential for a damaged tip during use of a laser probe.",
      "root_cause_description": "Under Investigation by firm",
      "action": "On October 11, 2024 URGENT: MEDICAL DEVICE CORRECTION letters were sent to consignees. Actions Required:\nOur records indicate that your facility has purchased one or more of the affected products. Therefore, Olympus requires you to take the following actions:\n1. Carefully read the content of this notification.\n2. Examine your inventory and identify the above-listed device.\n3. You should not use the Cystoscope Outer sheath, 22.5 French with a GreenLight Laser for BPH therapy until further notice from Olympus. Add a copy of this letter to any on-hand copies of the Instructions for Use.\n4. Olympus requests that you acknowledge receipt of this letter. Acknowledge receipt of this letter through the Olympus web portal: a.\nGo to https://olympusamerica.com/recall\nb. Enter the recall number \"0460 \nc. Complete the form as instructed.\n5. If you have further distributed this product, identify your customers, and forward them this notification.\nOlympus requests that you report any complaints, including the device breaking off into the patient, or any associated injuries to the Technical Assistance Center (TAC) at 1- 800-848-9024 (option 1), and the FDA. Adverse events experienced with the use of this product may also be reported to the FDA s MedWatch Adverse Event Reporting program either online, by regular mail, or by fax.\nOlympus fully appreciates your prompt cooperation in addressing this situation. If you require additional information, please do not hesitate to contact me by phone at (647) 999-3203 from Monday through Friday, 9 am to 5 pm EDT, or by e-mail at Cynthia.Ow@olympus.com.",
      "product_quantity": "738 units",
      "distribution_pattern": "US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.",
      "openfda": {
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          "K860103",
          "K954614",
          "K843683",
          "K896505",
          "K790071",
          "K862424",
          "K801247",
          "K771918",
          "K771920",
          "K896008",
          "K771919",
          "K833859"
        ],
        "device_name": "Endoscope, Ac-Powered And Accessories",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1500",
        "device_class": "2",
        "registration_number": [
          "3013247477",
          "3011986317",
          "8010487",
          "3007960282",
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        "fei_number": [
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        ]
      }
    }
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}