{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Anasco",
      "address_1": "Rd # 402, Km 4.2",
      "reason_for_recall": "Certain Silicone TECNIS IOLs may be labeled with the incorrect diopter power.",
      "address_2": "",
      "product_quantity": "169 units",
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      "center_classification_date": "20140303",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Australia, Great Britain, Canada and Japan.",
      "state": "PR",
      "product_description": "AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002, diopter size: 16.0 and 21.0.    Indicated for primary implantation for the visual correction of aphakia in adult patients.",
      "report_date": "20140312",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AMO Puerto Rico Manufacturing, Inc.",
      "recall_number": "Z-1123-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67385",
      "termination_date": "20170419",
      "more_code_info": "",
      "recall_initiation_date": "20140128",
      "postal_code": "00610",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}