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Medical Device

SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

Recall date: 2026-07-29 · Source: FDA_DEVICE
Brand / Firm
KENT IMAGING, INC.
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
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.
Units affected
77
Description
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
View official recall notice →