FDA Medical devices recall ·
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA recall
- Recall number
- Z-2775-2026
- Date
- (initiated June 30, 2026)
- Company / brand
- Kent Imaging, Inc.
1210 8 St Sw Suite 300, Calgary, N/A, Canada - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 77
- Hazard tags
- Software
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Why was it recalled?
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 should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
Distribution
US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
States: Arkansas Arizona California District of Columbia Florida Georgia Iowa Illinois Indiana Kansas Nevada Pennsylvania Tennessee Texas Utah
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2775-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.