{
  "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",
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      "cfres_id": "64540",
      "product_res_number": "Z-0106-2008",
      "event_date_initiated": "2007-09-20",
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      "recall_status": "Terminated",
      "event_date_terminated": "2008-02-15",
      "res_event_number": "44929",
      "product_code": "LQC",
      "k_numbers": [
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      "product_description": "Olympus Single Use Mechanical Lithotriptor, Model number BML-V232QR-30, Olympus America, Inc.",
      "code_info": "Model number BML-V232QR-30: Lot numbers 75K, 76K, and 77K.",
      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus America Inc.",
      "address_1": "3500 Corporate Pkwy.",
      "address_2": "P.O. Box 610",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-0610",
      "additional_info_contact": "Laura Storms-Tyler\n484-896-5688",
      "reason_for_recall": "Slider knob does not move smoothly causing the user difficulty in advancing the coil sheath",
      "root_cause_description": "Process control",
      "action": "The recalling firm issued a recall letter dated 9/20/07 to the medical facilities informing them of the problem and the need to return the product. The letter also informed the hospitals that replacement products would be sent.",
      "product_quantity": "201 units",
      "distribution_pattern": "Nationwide",
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        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4500",
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