FDA Device recall Z-2108-2021
3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Tele…
- FDA Device
- Class III
- terminated
- Published 2021-07-28
On 2021-07-28 the FDA classified a Class III recall of 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Tele… by Mindray Ds Usa, citing telepack may not power on when using the 3AA battery cradle.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2108-2021 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2021-05-27 |
| Published | 2021-07-28 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Mindray Ds Usa |
| Distribution | US |
Product
3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.
Reason
Telepack may not power on when using the 3AA battery cradle.
Identifiers
| code_info | Part Number 045-001699-01; Awaiting additional details |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2108-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.