{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Ontario",
      "address_1": "4290 E Brickell St Ste A",
      "reason_for_recall": "Aaren Scientific is recalling intraocular lenses because the instructions for use (IFU) are not fully compliant with US requirements.",
      "address_2": "",
      "product_quantity": "28 units",
      "code_info": "Serial No. 1181331102, 1181321102, 1393231208, 1117161211, 1180941102, 1031031102, 1190261307, 1190231307, 1190091307, 1190101307, 1190431307, 1190441307, 1276591307, 1305951307, 119071307, 1176951102, 1192921102, 1277111307, 1189541307, 1189551307, 1187761307, 1189531307, 1309911307, 1277101307, 1181331102, 1181321102, 1393231208, 1117161211, 1180941102, 1031031102, 1190261307, 1190231307, 1190091307, 1190101307, 1190431307, 1190441307, 1276591307, 1305951307, 1190071307, 1176951102, 1192921102, 1277111307, 1189541307, 1189551307, 1187761307, 1189531307, 1309911307, 1277101307, 1276941307, 1309961307.",
      "center_classification_date": "20150320",
      "distribution_pattern": "Distributed in the states of OK, KS, FL, and AL.",
      "state": "CA",
      "product_description": "Intraocular Lens (IOL), Part No. EC-3 PAL, Diopter: 17.5, 18.0, 18.5, 19.0, 19.5, 21.5, 23.5, 9.0, 22.5, 23.0, 21.0, 24.0.     The device is indicated for primary implantation in the capsular bag of the eye for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed. Aaren Scientific\u0019s EC-3 IOLs are intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia in adult patients in whom a cataractous lens has been removed by phacoemulsification.",
      "report_date": "20150401",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Aaren Scientific, Incorporated",
      "recall_number": "Z-1309-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70557",
      "termination_date": "20150629",
      "more_code_info": "",
      "recall_initiation_date": "20150213",
      "postal_code": "91761-1569",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}