Kent Imaging, Inc.: Autofluorescence Imaging Adjunct Tool For Wounds
Recall Summary Kent Imaging's SnapshotGLO Wound Imaging Device (Models KB100 and KB100AA) is being recalled because a software problem prevents the device from charging after its battery fully drains into a low-power shipping mode. When this happens, the device stops working for wound imaging until the issue is fixed. This Class II recall affects devices distributed across the United States.
- Recalling firm
- KENT IMAGING, INC.
- 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-30
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ccc21bbc-4730-4d18-b0e9-ec7959edab94