{
  "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": "2026-04-15",
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  "results": [
    {
      "country": "United States",
      "city": "Santa Ana",
      "address_1": "1700 E Saint Andrew Pl",
      "reason_for_recall": "Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they were not being checked prior to release and this may result in the release of mislabeled IOLs.",
      "address_2": "",
      "product_quantity": "217 units",
      "code_info": "Serial No.  7138841403  2648831412  2648971412  2649011412  2649071412  2649101412  2649181412  2649221412  2649241412  2649261412  2649281412  2649301412  7138301403  7138311403  7138321403  7138331403  7138341403  7138351403  7138361403  7138371403  7138381403  7138391403  7138401403  7138411403  7138431403  7138441403  7138451403  7138461403  7138471403  7138481403  7138491403  7138501403  7138511403  7138521403  7138531403  7138541403  7138551403  7138561403  7138571403  7138581403  7138591403  7138601403  7138611403  7138621403  7138631403  7138641403  7138651403  7138661403  7138671403  7138681403  7138691403  7138701403  7138711403  7138721403  7138731403  7138741403  7138751403  7138761403  7138771403  7138781403  7138791403  7138801403  7138811403  7138821403  7138831403  7138851403  7138881403  7138891403  7138901403  7138911403  7138921403  7138941403  7138951403  7138961403  7138971403  7138981403  7138991403  7139001403  7139011403  7139021403  7139031403  7139041403  7139051403  7139061403  7139071403  7139081403  7139091403  7139101403  7139111403  7139121403  7139131403  7139141403  2648751412  2648761412  2648771412  2648781412  2648791412  2648801412  2648811412  2648821412  2648841412  2648851412  2648861412  2648871412  2648881412  2648891412  2648901412  2648911412  2648921412  2648931412  2648941412  2648951412  2648961412  2648981412  2648991412  2649001412  2649021412  2649031412  2649041412  2649061412  2649081412  2649091412  2649111412  2649121412  2649131412  2649141412  2649151412  2649161412  2649171412  2649191412  2649201412  2649211412  2649231412  2649251412  2649271412  2649291412  2649311412  2397761605  2397981605  3125171501  3125181501  7731731310  7731741310  7731751310  7731761310  7731771310  7731781310  7731791310  7731801310  7731811310  7731821310  7731831310  7731841310  7731851310  7731861310  7731871310  7731881310  7731891310  7731901310  7731911310  7731921310  7731931310  7731941310  7731951310  7731961310  7731971310  7731981310  7731991310  7732001310  7732011310  7732021310  7732031310  7732041310  7732051310  7732061310  7732071310  7732081310  7732091310  7732101310  7732121310  7732131310  7732141310  7732151310  7732161310  7732181310  7732191310  7732201310  7732211310  7732221310  7732231310  7732241310  7732251310  7732261310  7732271310  7732281310  7732291310  7732301310  7732311310  7732321310  7732331310  7732341310  7732361310  7732371310  7732391310  7732401310  7732411310  7732421310  7732431310  7732441310  7732451310  7732461310  7732471310  7732481310  7732491310  7732501310  7732511310  7732521310",
      "center_classification_date": "20160921",
      "distribution_pattern": "Worldwide Distribution - US nationwide, PR, and Internationally to Canada, Latin America, Europe, Africa, Middle East, and Asia Pacific.",
      "state": "CA",
      "product_description": "TECNIS 1-Piece IOL with the TECNIS iTec Preloaded Delivery System, Model No. PCB00  The product is indicated for implantation for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by extracapsular cataract extraction. The lens is intended to be placed in the capsular bag.",
      "report_date": "20160928",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Abbott Medical Optics Inc. (AMO)",
      "recall_number": "Z-2861-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75051",
      "termination_date": "20161223",
      "more_code_info": "",
      "recall_initiation_date": "20160826",
      "postal_code": "92705-4933",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}