# FDA recall Z-2775-2026

> **KENT IMAGING, INC.** · Class II · device recall initiated 2026-06-30.

## 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.

## Distribution

US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.

## Key facts

- **Recall number:** Z-2775-2026
- **Recalling firm:** KENT IMAGING, INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-06-30
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Calgary, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2775-2026

## Citation

> AI Analytics. FDA recall Z-2775-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/Z-2775-2026. Source: US FDA. Licensed CC0.

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