{
  "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": "Mentor",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71048",
      "recalling_firm": "Volk Optical Inc",
      "address_1": "7893 Enterprise Dr",
      "address_2": "N/A",
      "postal_code": "44060-5309",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution to VA only",
      "recall_number": "Z-2055-2015",
      "product_description": "Lombart 90D Clear with case  Visualization during diagnosis and laser therapy of the human retina (fundus) using a slit lamp.",
      "product_quantity": "78 units",
      "reason_for_recall": "Mislabeling.  The incorrect lot number was engraved on the anodized aluminum ring.  The correct lot number is BE03356; however, BD03356 was engraved on the ring in error.",
      "recall_initiation_date": "20150227",
      "center_classification_date": "20150709",
      "termination_date": "20160204",
      "report_date": "20150715",
      "code_info": "Model: L90C, Lot: BE03356,"
    }
  ]
}