Class II — KENT IMAGING, INC.
| Recalling firm | Kent Imaging Inc. |
|---|---|
| Registered facility | Kent Imaging Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | SnapshotGLO Wound Imaging Device, Model KB100, KB100AA. |
| Quantity | 77 |
| Distribution | US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ. |
| Initiated | 2026-06-30 |
| Classified | 2026-07-22 |
| Recall number | Z-2775-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — KENT IMAGING, INC. (Z-2775-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99406/
Alerts for Kent Imaging Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.