Kent Imaging, Inc.: Snapshotglo Wound Imaging Device, Model Kb100, Kb100aa
SnapshotGLO Wound Imaging Device Recall Summary Kent Imaging is recalling SnapshotGLO Wound Imaging Devices (Models KB100 and KB100AA) because the software controlling the battery charging circuit cannot recognize when a battery has fully discharged into shipping mode, preventing the device from charging and becoming temporarily unusable. The affected devices were distributed nationwide to healthcare facilities in multiple states. This is classified as a Class II recall, meaning the problem could result in temporary loss of device function.
- 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
- U.S. Food and Drug Administration
- Recall date
- 2026-06-30
- Status
- Ongoing
- 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 U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/aa7ea71f-1bc3-4f2b-bd41-9f35e8c8aac0