Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2775-2026 — SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

U.S. FDA — Device Enforcement · Canada · 2026-06-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2775-2026
Date of alert
2026-06-30
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
KENT IMAGING, INC.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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