---
title: "SnapshotGLO Wound Imaging Device, Model KB100, KB100AA. — FDA record Z-2775-2026 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-2775-2026-snapshotglo-wound-imaging-device-model-kb100-kb100aa/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# SnapshotGLO Wound Imaging Device, Model KB100, KB100AA. — FDA record Z-2775-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 30, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Recalling firm**: KENT IMAGING, INC.
- **Quantity**: 77
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2775-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2775-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI-DI: B376KB1000, Software Revisions v4.2.0 and v4.1.3 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Indiana](https://isitonrecall.com/state/indiana/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jul 29, 2026
- **Recall initiation date**: Jun 30, 2026
- **Center classification date**: Jul 22, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2775-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [KENT IMAGING, INC. records](https://isitonrecall.com/brand/kent-imaging-inc/)