Medical Device Recall: SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
KENT IMAGING, INC. · June 30, 2026
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.
Distribution
US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
States Affected
NATIONWIDE
Quantity Affected
77
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2775-2026
Status: ongoing
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