FDAFDA recall Z-2775-2026 · Jul 29, 2026
KENT IMAGING, INC.: SnapshotGLO Wound Imaging Device recall
Recall found
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Reason for recall
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
- Quantity
- 77
- Distribution
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
- Recalling firm
- KENT IMAGING, INC., Calgary, N/A
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-30
Source: openFDA enforcement record Z-2775-2026 · search recall number Z-2775-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.