KENT IMAGING recalls

Recall found. KENT IMAGING is named in FDA Class II recall Z-2775-2026 covering SnapshotGLO Wound Imaging Device. 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. Status: Ongoing.

Models with recalls

SnapshotGLO Wound Imaging Device (1)

All KENT IMAGING recalls

FDA Class II · Medical device · July 29, 2026

SnapshotGLO Wound Imaging Device recall — KENT IMAGING, INC.

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…

Official ID Z-2775-2026 · Official record ↗

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.