TemporaryFDAOngoing
Can cause harm that is usually temporary.
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Check the device or its packaging for
UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
- Why
- 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.
- Distributed
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
- Company
- KENT IMAGING, INC.
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-2775-2026 · retrieved 22 July 2026
Read the official notice