{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88826",
      "recalling_firm": "Beaver Visitec International, Inc.",
      "address_1": "500 Totten Pond Rd",
      "address_2": "10 City Point",
      "postal_code": "02451-1916",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Foreign: Australia Austria  France  Germany  Netherlands  Spain Japan Russia  South Africa UK",
      "recall_number": "Z-0230-2022",
      "product_description": "bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587",
      "product_quantity": "2 units",
      "reason_for_recall": "Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades",
      "recall_initiation_date": "20211008",
      "center_classification_date": "20211116",
      "report_date": "20211124",
      "code_info": "Lot Number 6018382",
      "more_code_info": ""
    }
  ]
}