KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device
- Recalling company
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Jun 30, 2026
- Reported
- Jul 29, 2026
- Distribution
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
- Status
- Ongoing
- Quantity
- 77
- Lot / codes
- UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
- Company location
- Calgary, N/A
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2775-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2775-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.