{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "cfres_id": "45523",
      "product_res_number": "Z-0847-06",
      "event_date_initiated": "2006-04-12",
      "event_date_posted": "2006-05-06",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-09-13",
      "res_event_number": "35214",
      "product_code": "KYF",
      "k_numbers": [
        "K905703"
      ],
      "product_description": "Valve-EV Glaucoma Ultra-Smooth, P/N 6006",
      "code_info": "Serial numbers:  11102A through 11107A",
      "firm_fei_number": "1000022662",
      "recalling_firm": "Eagle Vision Inc",
      "address_1": "8500 Wolf Lake Dr Ste 110 8500 Wolf Lake Dr",
      "address_2": "Ste 110",
      "city": "Memphis",
      "state": "TN",
      "postal_code": "38133-4104",
      "additional_info_contact": "Wade Allen\n901-380-7000",
      "reason_for_recall": "Product may have deformed valves which would cause the valve not to operate properly.",
      "root_cause_description": "Other",
      "action": "Written notification of the recall was sent out beginning 04/12/2006 to hospital administrators to advise them of the recall.  The letter stated that implanting physicians were to be notified.  A second updated notice was sent dated 04/19/2006 which contained more detailed information regarding the product problem.",
      "product_quantity": "6 units",
      "distribution_pattern": "Nationwide, Canada, Columbia, Turkey, & The Netherlands",
      "openfda": {
        "k_number": [
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        ],
        "registration_number": [
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        ],
        "device_name": "Implant, Eye Valve",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.3920",
        "device_class": "2"
      }
    }
  ]
}