# FDA recall Z-2471-2021

> **Siemens Medical Solutions USA, Inc.** · Class II · device recall initiated 2021-07-12.

## 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.

## Distribution

Worldwide distribution - U.S. Nationwide distribution in the Puerto Rico and the countries of Bosnia Herzegovina, Canada, Colombia, Germany, Greece, Italy, North Macedonia, Poland, and Slovenia.

## Key facts

- **Recall number:** Z-2471-2021
- **Recalling firm:** Siemens Medical Solutions USA, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-07-12
- **Report date:** 2021-09-22
- **Termination date:** 2024-10-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Issaquah, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2471-2021

## Citation

> AI Analytics. FDA recall Z-2471-2021. Retrieved 2026-07-11 from https://api.ai-analytics.org/recall/Z-2471-2021. Source: US FDA. Licensed CC0.

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