# FDA recall Z-0554-2018

> **Mindray DS USA, Inc. dba Mindray North America** · Class II · device recall initiated 2017-07-14.

## Product

TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00

## Reason for recall

A damaged circuit board in the battery charger can cause the battery to overcharge and the battery case to swell and separate.

## Distribution

Distributed in 26 states: AL, CA, CO, FL, GA, IA, IN, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, PA, SD, TX, UT, WA, and WY; and Puerto Rico.

## Key facts

- **Recall number:** Z-0554-2018
- **Recalling firm:** Mindray DS USA, Inc. dba Mindray North America
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-07-14
- **Report date:** 2018-02-14
- **Termination date:** 2018-12-17

- **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-0554-2018

## Citation

> AI Analytics. FDA recall Z-0554-2018. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0554-2018. Source: US FDA. Licensed CC0.

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