# FDA recall Z-0789-2024

> **KENT IMAGING, INC.** · Class II · device recall initiated 2023-10-30.

## Product

Snapshot NIR, REF: KD204

## Reason for recall

Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.

## Distribution

Worldwide - US Nationwide distribution in the states of IN, OH, TX, PA, WI, OR, CO, IL, MO, CA, AZ, IA and the countries of Malaysia.

## Key facts

- **Recall number:** Z-0789-2024
- **Recalling firm:** KENT IMAGING, INC.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-30
- **Report date:** 2024-01-31

- **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-0789-2024

## Citation

> AI Analytics. FDA recall Z-0789-2024. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0789-2024. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*