{
  "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": "2026-04-22",
    "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": "64410",
      "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": "Worldwide Distribution - USA including the states of AZ, CA, GA, MN, NJ, and NM.  Internationally to Japan.",
      "recall_number": "Z-0966-2013",
      "product_description": "20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens    For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.",
      "product_quantity": "40 devices",
      "reason_for_recall": "The defect was with mis-engraving of the lot # directly on the product and it\u0019s packaging. Mixed up device engraving of V20LC (lot # BB09213) with that from V60C (lot # BB09205).",
      "recall_initiation_date": "20121025",
      "center_classification_date": "20130318",
      "termination_date": "20130611",
      "report_date": "20130327",
      "code_info": "Product Code:  V20LC; Lot/Serial Numbers:  BB09213 & BB09205"
    }
  ]
}