{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Waltham",
      "address_1": "411 Waverley Oaks Rd Ste 229",
      "reason_for_recall": "Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product",
      "address_2": "",
      "product_quantity": "621 kits",
      "code_info": "Lot Numbers: 3035614  3046205  3052693  3055885  3063181  3068806  3073917  3082315",
      "center_classification_date": "20150615",
      "distribution_pattern": "Nationwide Distribution including KY, GA, MI, and NJ.",
      "state": "MA",
      "product_description": "BVI Custom Eyes¿ Ophthalmic Procedure Kits with the component -Devon Light Glove  Part Number: 584569  Ophthalmic surgical kits",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Beaver-Visitec International Inc.",
      "recall_number": "Z-1802-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71293",
      "termination_date": "20210128",
      "more_code_info": "",
      "recall_initiation_date": "20150501",
      "postal_code": "02452-8422",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}