{
  "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": "Calgary",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99406",
      "recalling_firm": "KENT IMAGING, INC.",
      "address_1": "1210 8 St Sw Suite 300",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.",
      "recall_number": "Z-2775-2026",
      "product_description": "SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.",
      "product_quantity": "77",
      "reason_for_recall": "The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power \"shipping mode.\" When this occurs, an affected device will not resume charging when reconnected to power and becomes temporarily unusable/ unavailable for wound imaging until corrected.",
      "recall_initiation_date": "20260630",
      "center_classification_date": "20260722",
      "report_date": "20260729",
      "code_info": "UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3"
    }
  ]
}