Vios Monitoring System Bedside Monitor Model BSM2050 — Class II medical device recall Z-1292-2025
Ongoing recall by Murata Vios, Inc., reported 2025-03-12, distributed nationwide. Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet
| Recall number | Z-1292-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Murata Vios, Inc., Woodbury, MN, United States |
| Recall initiated | 2024-08-09 |
| Classified | 2025-03-06 |
| Reported by FDA | 2025-03-12 |
| Distributed | Nationwide (US) |
| Quantity | 50 |
| Model numbers | BSM2050 |
Product
Vios Monitoring System Bedside Monitor Model BSM2050
Reason for recall
Batteries may deplete over time while not in use if devices are stored without being plugged in to wall outlet. Depleted batteries may lead to tablet connectivity issues.
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-1292-2025. 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.