FDAFDA · Food and drugs·Recall number Z-2775-2026
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Published July 29, 2026 · Recall initiated: June 30, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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
Voluntary: Firm initiated
Recall details
- Manufacturer
- KENT IMAGING, INC.
- Distributor
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
- Lot
- UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Canada
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