FDA Device recall Z-2775-2026
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA
- FDA Device
- Class II
- ongoing
- Published 2026-07-29
On 2026-07-29 the FDA classified a Class II recall of SnapshotGLO Wound Imaging Device, Model KB100, KB100AA by Kent Imaging, citing 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 "shippi….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2775-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-30 |
| Published | 2026-07-29 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Kent Imaging |
| Distribution | US |
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Reason
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.
Identifiers
| code_info | UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2775-2026%22
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