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KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Recalled July 29, 2026 · FDA recall Z-2775-2026 · KENT IMAGING
Hazard
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. · FDA Class II
Units
77
Sold at
US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
Description
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.
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Manufacturer(s)
KENT IMAGING, INC.
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →