Drug recall
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
FDA recall event 68646 · Class II · Karl Storz Endoscopy
Key facts
| Event ID | 68646 |
|---|---|
| Recall numbers | Z-2039-2014 |
| Recalling firm | Karl Storz Endoscopy |
| Product type | Devices |
| Products | Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | KARL STORZ Endoscopy-America is recalling the Essential NEO because the connected power cable could potentially become overheated and result in smoke being generated and the cessation of function of… |
| Initiation date | Jun 25, 2014 |
| Report date | Jul 16, 2014 |
| Termination date | Jan 13, 2015 |
| City | El Segundo |
| State | CA |
| Country | United States |
| FEI number | 3007475226 |
At a glance
- 1–9 Products in this recall
- 1–9 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: