{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "220717",
      "product_res_number": "Z-2675-2026",
      "event_date_initiated": "2026-04-06",
      "event_date_posted": "2026-07-21",
      "recall_status": "Open, Classified",
      "res_event_number": "99059",
      "product_code": "REU",
      "product_description": "The intended use is to be paired with a weapon for aiming purposes.",
      "code_info": "None provided.",
      "firm_fei_number": "3007858386",
      "recalling_firm": "Wilcox Industries Corp.",
      "address_1": "25 Piscataqua Dr",
      "city": "Newington",
      "state": "NH",
      "postal_code": "03801-7816",
      "reason_for_recall": "Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be returned to implement this change.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be returned to implement this change. Wilcox provided customers with contact information for our customer service as well to help facilitate returns and any questions.\nIf this involved a medical device, has a Medical Device Report (MDR) been submitted to FDA?* Yes No N/A Unknown\nOther Important",
      "distribution_pattern": "US Nationwide distribution in the state of NH.",
      "openfda": {
        "device_name": "Laser Aiming Product, Visible",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}