Mindray DS USA, Inc. dba Mindray North America: Medical Device Recall in 2018 - (Recall #: Z-0554-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 14, 2017

Date Posted: February 14, 2018

Recall Number: Z-0554-2018

Event ID: 79005

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.

Status: Terminated

Product Quantity: 203

Code Information:

All battery chargers with part number 115-030108-00

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated