Drug recall
SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by…
FDA recall event 67153 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 67153 |
|---|---|
| Recall numbers | Z-0786-2014 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto now known as Mecasim Parc de l Esplanade 9,Rue Niels Bohr 77400 Saint Thibault des… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | In a very rare occurrence an intended movement of the SimView NT simulation system components could not be stopped with usual hand control or the collision detection functionality. |
| Initiation date | Dec 11, 2013 |
| Report date | Jan 29, 2014 |
| Termination date | Mar 31, 2014 |
| City | Martinez |
| State | CA |
| Country | United States |
| FEI number | 2910081 |
At a glance
- 1–9 Products in this recall
- None 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: