{
  "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": "214 kits",
      "code_info": "Lot Numbers:   3045852  3053258  3063193  3068829",
      "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: 584671  Ophthalmic surgical kits",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Beaver-Visitec International Inc.",
      "recall_number": "Z-1805-2015",
      "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"
    }
  ]
}