Drug recall
V5Ms Transesophageal transducers; V5Ms trans-esophageal echocardiograph (TEE) ultrasound transducer is…
FDA recall event 69138 · Class II · Siemens Medical Solutions USA, Inc.
Key facts
| Event ID | 69138 |
|---|---|
| Recall numbers | Z-2571-2014 |
| Recalling firm | Siemens Medical Solutions USA, Inc. |
| Product type | Devices |
| Products | V5Ms Transesophageal transducers; V5Ms trans-esophageal echocardiograph (TEE) ultrasound transducer is intended primarily for cardiology applications |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Reports of deterioration of material covering the articulating section of the V5Ms transesophageal transducer. |
| Initiation date | Aug 13, 2014 |
| Report date | Sep 10, 2014 |
| Termination date | Mar 6, 2015 |
| City | Mountain View |
| State | CA |
| Country | United States |
| FEI number | 2936884 |
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: