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SnapshotGLO Wound Imaging Device
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MEDICAL DEVICE RECALLMODERATE

SnapshotGLO Wound Imaging Device

Kent Imaging recalls SnapshotGLO wound imaging devices due to battery charging failure.

What to do

Stop using the affected device and contact Kent Imaging for a replacement or repair.

Recalled
Listed
Updated
Recall No.
Z-2775-2026
Agency
FDA
Firm
KENT IMAGING, INC.
Recall ID
99406
Status
ONGOING

Why it was recalled

Kent Imaging is recalling the SnapshotGLO Wound Imaging Device, Model KB100 and KB100AA, because the battery charging circuit software cannot recover a battery that has fully discharged into shipping mode, rendering the device temporarily unusable for wound imaging.

Is mine affected?

This recall covers the product below. If you have it, yours is affected.

SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

Other Software Defect recalls

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Editorial summary by Recall Canary · summary updated 2026-07-23 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification