Drug recall
ACUSON Juniper Diagnostic Ultrasound System
FDA recall event 88405 · Class II · Siemens Medical Solutions USA, Inc.
Key facts
| Event ID | 88405 |
|---|---|
| Recall numbers | Z-2471-2021 |
| Recalling firm | Siemens Medical Solutions USA, Inc. |
| Product type | Devices |
| Products | ACUSON Juniper Diagnostic Ultrasound System |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable. |
| Initiation date | Jul 12, 2021 |
| Report date | Sep 22, 2021 |
| Termination date | Oct 16, 2024 |
| City | Issaquah |
| State | WA |
| Country | United States |
| FEI number | 3023245 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: