# FDA recall Z-2175-2025

> **Remote Diagnostic Technologies Ltd.** · Class II · device recall initiated 2025-05-30.

## Product

Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an accessory to the Tempus Pro Monitor, REF: 00-1007-R, 00-1024-R, 00-1026-R

## Reason for recall

Kit USB flash drive contains outdated software, which could result in reverting patient monitor to outdated software and reintroducing the video laryngoscope issue (related to an August 2023 recall), which could lead to delay in diagnosis, delayed treatment, hypoxia due to unexpected loss of video laryngoscopy and all other monitor measurements during system restart.

## Distribution

Worldwide - US Nationwide distribution in the states of SC, KY, NV, IA, MI and the country of  GB.

## Key facts

- **Recall number:** Z-2175-2025
- **Recalling firm:** Remote Diagnostic Technologies Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-30
- **Report date:** 2025-08-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Farnborough, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2175-2025

## Citation

> AI Analytics. FDA recall Z-2175-2025. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-2175-2025. Source: US FDA. Licensed CC0.

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