TI Transport Monitor/Module Battery Pack Product Usage: intended for… — Class II medical device recall Z-2634-2017
Terminated recall by Mindray DS USA, Inc. dba Mindray North America, reported 2017-07-05, distributed nationwide. Mindray has received two reports from outside the United States that the battery pack for TI transport monitor
| Recall number | Z-2634-2017 |
|---|---|
| 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 | 2017-04-28 |
| Classified | 2017-06-27 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2019-03-22 |
| Distributed | Nationwide (US) |
| Quantity | 2,718 batteries |
| Reason classes | device malfunction |
Product
TI Transport Monitor/Module Battery Pack Product Usage: intended for monitoring, displaying, reviewing, storing, alarming and transferring of multiple physiological parameters.
Reason for recall
Mindray has received two reports from outside the United States that the battery pack for TI transport monitor/module overheated.
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-2634-2017. 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.