{
  "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": "585 kits",
      "code_info": "Lot Numbers:   3039720  3046211  3047770  3049473  3070763  3082330  3089827  3093682  3095941  3106407  3117874",
      "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: 584649  Ophthalmic surgical kits",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Beaver-Visitec International Inc.",
      "recall_number": "Z-1804-2015",
      "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"
    }
  ]
}