{"url_path":"/fda/device/recalls/Z-2775-2026","section_key":"summary","section_title":"DEVICE Recall: KENT IMAGING, INC. — SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-06-30","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2775-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"KENT IMAGING, INC."},"word_count":121,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2775-2026\n\n**Recalling firm:** KENT IMAGING, INC.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-06-30\n**Report date:** 2026-07-29\n\n## Product\nSnapshotGLO Wound Imaging Device, Model KB100, KB100AA.\n\n## Reason\nThe 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.\n\n## Affected lots\nUDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3\n\n## Distribution\nUS Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ."}