# FDA recall Z-2634-2017

> **Mindray DS USA, Inc. dba Mindray North America** · Class II · device recall initiated 2017-04-28.

## Product

TI Transport Monitor/Module Battery Pack    Product Usage:  intended for monitoring, displaying, reviewing, storing, alarming and transferring of multiple physiological parameters.

## Reason for recall

Mindray has received two reports from outside the United States that the battery pack for TI transport monitor/module overheated.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-2634-2017
- **Recalling firm:** Mindray DS USA, Inc. dba Mindray North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-04-28
- **Report date:** 2017-07-05
- **Termination date:** 2019-03-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2634-2017

## Citation

> AI Analytics. FDA recall Z-2634-2017. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2634-2017. Source: US FDA. Licensed CC0.

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