⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

KENT IMAGING, INC.: SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

Medical DevicesSource: FDA (device) · Date: 2026-07-29

Read the official notice at FDA (device) →

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The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
KENT IMAGING, INC.
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Reason / 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.
Classification
Class II
Status
Ongoing
Distribution / sold at
US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
Recall initiated
2026-06-30
Code info
UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
Product quantity
77
Voluntary mandated
Voluntary: Firm initiated
City
Calgary
State
N/A
Country
Canada
Event id
99406
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