FDA Device recall Z-0554-2018
TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
- FDA Device
- Class II
- terminated
- Published 2018-02-14
On 2018-02-14 the FDA classified a Class II recall of TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00 by Mindray Ds Usa, citing A damaged circuit board in the battery charger can cause the battery to overcharge and the battery case to swell and separate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0554-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-14 |
| Published | 2018-02-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Mindray Ds Usa |
| Distribution | AL, CA, CO, FL, GA, IA, IN, ME, MI, MN, MO, NC, ND, NE, NH, NJ, NM, NV, NY, OH, PA, PR, SD, TX, UT, WA, WY |
Product
TD60 Transmitter battery charger used with the BeneVision Central Station, Part number 115-030108-00
Reason
A damaged circuit board in the battery charger can cause the battery to overcharge and the battery case to swell and separate.
Identifiers
| code_info | All battery chargers with part number 115-030108-00 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0554-2018%22
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