Recall
FDAHealthJune 30, 2026

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

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 30, 2026

US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.

What's affected?

Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Lot code
UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3

Additional details

UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 77.

View original FDA notice →

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