Notice names this product. KENT IMAGING’s SnapshotGLO Wound Imaging Device is named in FDA Class II recall Z-2775-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: 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. Identifying details: UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3. Units affected: 77. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
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 "shippin…
Company / brand: KENT IMAGING
Affected product: SnapshotGLO Wound Imaging Device
Official ID Z-2775-2026 · Official record ↗
See all KENT IMAGING recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.