{
  "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": [
    {
      "country": "United States",
      "city": "Mentor",
      "address_1": "7893 Enterprise Dr",
      "reason_for_recall": "The firm discovered that the incorrect lot number was engraved on the product.",
      "address_2": "",
      "product_quantity": "9 lens",
      "code_info": "Model #: VG4SNF, Lot: BE05200",
      "center_classification_date": "20160315",
      "distribution_pattern": "Worldwide Distribution - US (Virginia only) Internationally to Canada, France & Indonesia.",
      "state": "OH",
      "product_description": "Volk G-4 Small Ring, No Flange, Gonio Lens with case, UPC: 811608013602  for use as diagnostic contact lenses for eye examinations (including the anterior chamber, trabecular meshwork, central retina, and peripheral retina) and use in the therapy of intraocular abnormalities",
      "report_date": "20160323",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Volk Optical Inc",
      "recall_number": "Z-1177-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73213",
      "termination_date": "20170426",
      "more_code_info": "",
      "recall_initiation_date": "20160202",
      "postal_code": "44060-5309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}