{
  "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": "2026-08-13",
    "results": {
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      "product_res_number": "Z-0051-05",
      "event_date_initiated": "2004-04-12",
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      "recall_status": "Terminated",
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      "res_event_number": "29903",
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      "address_1": "33 Technology Dr",
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      "additional_info_contact": "Elizabeth L. MacAdams, CQA, RAC\n800-370-4632",
      "reason_for_recall": "Anaphylactic-like reactions were reported following repeated cystoscopy for bladder cancer patients where the scope had been reprocessed in CIDEX OPA Solution.",
      "root_cause_description": "Other",
      "action": "Firm conducted WebEx meeting with affiliates on  April 12 & 13, 2004 to discuss CIDEX OPA Solution labeling.  April 23, 2004, Firm sent letters to affiliates, customers, and end users to notify of new contraindication for CIDEX OPA Solution.  Same letter was sent to U.S. Healthcare facilities on April 23, 2004; to Urology M.D.s on April 28, 2004; to Urologist Nurses on May 7, 2004.\nCustomers can call 800-370-4632 with questions.",
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        "device_name": "Sterilant, Medical Devices",
        "medical_specialty_description": "General Hospital",
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