{
  "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": {
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  "results": [
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      "cfres_id": "50119",
      "product_res_number": "Z-0431-2007",
      "event_date_initiated": "2006-12-14",
      "event_date_posted": "2007-02-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-04-09",
      "res_event_number": "37009",
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      "recalling_firm": "Alcon Laboratories, Inc",
      "address_1": "6201 South Fwy",
      "city": "Fort Worth",
      "state": "TX",
      "postal_code": "76134-2001",
      "reason_for_recall": "Intraocular lenses exposed to extreme temperatures while in storage.",
      "root_cause_description": "Other",
      "action": "The recall of the fifteen re-shipped lenses was conducted by telephone calls to the nine customers that had received the lenses.  These calls were made on December 14, 2006.",
      "product_quantity": "one unit",
      "distribution_pattern": "Nationwide.",
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        "device_name": "Lens, Multifocal Intraocular",
        "medical_specialty_description": "Ophthalmic",
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