{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Aliso Viejo",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81812",
      "recalling_firm": "RVO 2.0, INC",
      "address_1": "26800 Aliso Viejo Pkwy",
      "address_2": "Ste 160",
      "postal_code": "92656-2625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S.: NV, GA, NY, MN, TX, ND, AZ, VA, SD, IN, MA, MO, CA, NC, UT, IL, NH, OH, OK, FL, NJ, TN, MI, PA, HI, ID, KY, NE, AL, LA, CO, MD, MS, OR, WI, AR, WA;    No OUS (Foreign) Distribution.",
      "recall_number": "Z-0865-2019",
      "product_description": "Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.",
      "product_quantity": "2869",
      "reason_for_recall": "During a post approval study the firm found there was an increased risk of corneal haze following the implantation of this device.",
      "recall_initiation_date": "20181113",
      "center_classification_date": "20190305",
      "termination_date": "20240314",
      "report_date": "20190313",
      "code_info": "All lots of unused product"
    }
  ]
}