FDA recall Z-2775-2026

KENT IMAGING, INC. · Class II · device

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.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2026-06-30
Report date
2026-07-29
Voluntary/Mandated
Voluntary: Firm initiated
Location
Calgary, N/A, Canada

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2775-2026