{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "49638",
      "product_res_number": "Z-0148-2007",
      "event_date_initiated": "2006-11-29",
      "event_date_posted": "2006-12-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-05-24",
      "res_event_number": "36943",
      "product_code": "HQL",
      "pma_numbers": [
        "P990080/S6"
      ],
      "product_description": "AMO Tecnis Acrylic Model ZA9003 Intraocular Lenses",
      "code_info": "Serial numbers: 531644065, 5316450605, 5316460605, 5316470605, 5316490605, 5316500605, and 5316510605",
      "firm_fei_number": "3003843509",
      "recalling_firm": "Advanced Medical Optics, Inc.",
      "address_1": "1700 E Saint Andrew Pl",
      "city": "Santa Ana",
      "state": "CA",
      "postal_code": "92705-4933",
      "additional_info_contact": "John Smith\n714-247-8691",
      "reason_for_recall": "The lenses are incorrectly labeled as 11 diopter lenses; these lenses are actually 22.5 diopters.",
      "root_cause_description": "Other",
      "action": "On November 13, 2006, an 'URGENT MEDICAL DEVICE RECALL' letter was mailed to all affected US customers communicating their recall strategy regarding the removal of five (5) ZA9003 lenses in US distribution.  This letter included in this correspondence is a listing of the serial numbers and the quantities of intraocular lenses shipped.\n\nThis listing will act as your Facsimile Form to be returned to AMO for accountability of the lenses shipped to your facility. AMO will ensure the effectiveness of the recall by using a return facsimile form to capture the status of each of the lenses.",
      "product_quantity": "10 lenses",
      "distribution_pattern": "Worldwide, including USA (CT, TX, NY), Canada, and UK.",
      "openfda": {
        "k_number": [
          "K913626",
          "K842504",
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          "K771933",
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          "P860059",
          "P880085",
          "P880082",
          "P080021",
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          "P040020",
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          "P900048",
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          "P900053",
          "P930014",
          "P810042",
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          "P840060",
          "P910058",
          "P800049",
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          "P800017",
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          "P840050",
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          "P890068",
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        ],
        "registration_number": [
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        "fei_number": [
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          "3002957101",
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        ],
        "device_name": "Intraocular Lens",
        "medical_specialty_description": "Ophthalmic",
        "regulation_number": "886.3600",
        "device_class": "3"
      }
    }
  ]
}