ACUSON Juniper Diagnostic Ultrasound System — Class II medical device recall Z-2471-2021
Terminated recall by Siemens Medical Solutions USA, Inc., reported 2021-09-22, distributed nationwide. Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable.
| Recall number | Z-2471-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc., Issaquah, WA, United States |
| Recall initiated | 2021-07-12 |
| Classified | 2021-09-14 |
| Reported by FDA | 2021-09-22 |
| Terminated | 2024-10-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO, DE, GR, IT, PL, SI |
| Quantity | 15 systems |
| UPC / GTIN / UDI-DI | 04056869152059 |
| Serial numbers | 550975, 552770, 553629, 553951, 555060, 555601, 555602, 555603, 555604, 555605, 555606, 555607, 555610, 555611, 555612, 555613, 555626 |
| Model numbers | 11335791 |
Product
ACUSON Juniper Diagnostic Ultrasound System
Reason for recall
Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable.
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-2471-2021. 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.