Medical device recalls Moderate risk

Mindray DS USA, Inc. dba Mindray North America recalls TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00

Recall date
July 14, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0554-2018
FDA classification
Class II
Brand / firm
Mindray DS USA, Inc. dba Mindray North America
Sold / distributed
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.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

Get recall alerts

Free email alert whenever Mindray DS USA, Inc. dba Mindray North America has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Mindray DS USA, Inc. dba Mindray North America