{
  "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",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "25651 Atlantic Ocean Dr Ste A1",
      "reason_for_recall": "ReVision Optics has updated the instructions for use (IFU) for the Raindrop Near Vision Inlay to emphasize that only Balanced Salt Solution (BSS) may be used to irrigate under the flap and that topical medications or lubricants should not be administered until centration of the inlay and proper flap positioning has been confirmed at the slit lamp.",
      "address_2": "",
      "product_quantity": "1,279 devices",
      "code_info": "multiple lots since 08/01/2016",
      "center_classification_date": "20170321",
      "distribution_pattern": "US: AL, AZ, CA, FL, GA, HI, IL, IN, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NY, OH, OK, PA, SD, TN, TX,  UT, WA",
      "state": "CA",
      "product_description": "Raindrop Near Vision Inlay, Model# RD1-1",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Revision Optics Inc",
      "recall_number": "Z-1518-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76422",
      "termination_date": "20170621",
      "more_code_info": "",
      "recall_initiation_date": "20170207",
      "postal_code": "92630-8835",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}