{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4
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  },
  "results": [
    {
      "cfres_id": "220044",
      "product_res_number": "Z-2718-2026",
      "event_date_initiated": "2026-05-05",
      "event_date_posted": "2026-07-10",
      "recall_status": "Open, Classified",
      "res_event_number": "98869",
      "product_code": "KQT",
      "product_description": "Olympus Toomey Evacuator 30cc with Adaptor. Model Number: 188.",
      "code_info": "Model Number: 188. UDI-DI: 00821925001053. All Lot Numbers.",
      "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": "Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Olympus notified consignees on about 06/05/2026 via Courier, 2-day delivery. Consignees were requested to examine inventory for affected units. If affected units are on hand, replace any existing sterilization instructions for these products with those provided with the notification and add these instructions to any existing copies of the IFU. Consignees were also instructed to acknowledge receipt of the customer letter through the web portal. If affected units were further distributed, Olympus instructed consignees to identify those customers and forward the notification to them. An updated notice was sent to consignees on 06/30/2026 with further clarification regarding instructions to be used to sterilize affected devices going forward.",
      "product_quantity": "190 units",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Japan, EU, and Latin America.",
      "openfda": {
        "device_name": "Evacuator, Gastro-Urology",
        "medical_specialty_description": "Gastroenterology, Urology",
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