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
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