{"recall":{"id":"fda-device-99406","source":"FDA","sourceName":"U.S. Food and Drug Administration (openFDA device enforcement)","cat":"medicines","kids":false,"kind":"device","title":"KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device","firm":"KENT IMAGING, INC.","date":"2026-06-30","reported":"2026-07-29","status":"Ongoing","classification":"Class II","products":[{"name":"SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.","code":"UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3","quantity":"77","number":"Z-2775-2026","classification":"Class II"}],"reason":"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.","hazard":"FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).","affected":"US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.","nationwide":true,"states":[],"units":"77","remedy":"","whatToDo":"Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.","contact":"","url":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99406","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","rawHash":"19c33546e832ce49","firstSeen":"2026-11-02T13:57:14.206Z","updatedAt":"2026-11-02T13:57:14.206Z","history":[]},"official":{"fetchedAt":"2026-11-02T13:57:14.206Z","apiUrl":"https://api.fda.gov/device/enforcement.json?search=report_date:[20260705+TO+20991231]&sort=report_date:desc&limit=1000","officialUrl":"https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99406","record":[{"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"}]}}