{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73343",
      "recalling_firm": "AcuFocus, Inc.",
      "address_1": "32 Discovery Ste 200",
      "address_2": "N/A",
      "postal_code": "92618-3161",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "International distribution in countries of: Canada, Germany, Saudi Arabia, Turkey, and United Kingdom.",
      "recall_number": "Z-1235-2016",
      "product_description": "KAMRA Inlay, ACI 7000 Corneal Inlay, Part No. 76195-01 and 76195-10    (OUS) Labeling: The KAMRA inlay is indicated for the improvement of near visual acuity in one eye (usually the non-dominant eye) of a presbyopic patient.",
      "product_quantity": "182 units",
      "reason_for_recall": "AcuFocus is recalling KAMRA ACI 7000 Corneal Inlays due to concerns with the labeled shelf life.",
      "recall_initiation_date": "20160211",
      "center_classification_date": "20160324",
      "termination_date": "20160504",
      "report_date": "20160330",
      "code_info": "Lots A534-1014 and A535-1014"
    }
  ]
}