TD60 Transmitter battery charger used with the BeneVision Central… — Class II medical device recall Z-0554-2018
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2018-02-14, distributed in AL, CA, CO, FL, GA, IA, IN, ME…. A damaged circuit board in the battery charger can cause the battery to overcharge and the battery case to swe
| Recall number | Z-0554-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mindray DS USA, Inc. dba Mindray North America, Mahwah, NJ, United States |
| Recall initiated | 2017-07-14 |
| Classified | 2018-02-08 |
| Reported by FDA | 2018-02-14 |
| Terminated | 2018-12-17 |
| Distributed | 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 |
| Quantity | 203 |
| Model numbers | 115-030108-00 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0554-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.