{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Newington",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99059",
      "recalling_firm": "Wilcox Industries Corp.",
      "address_1": "25 Piscataqua Dr",
      "address_2": "N/A",
      "postal_code": "03801-7816",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the state of NH.",
      "recall_number": "Z-2675-2026",
      "product_description": "The intended use is to be paired with a weapon for aiming purposes.",
      "product_quantity": "N/A",
      "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.",
      "recall_initiation_date": "20260406",
      "center_classification_date": "20260721",
      "report_date": "20260729",
      "code_info": "None provided."
    }
  ]
}