Recall Z-2039-2014— Karl Storz Endoscopy
Class II · Terminated
Class II FDA medical device recall by Karl Storz Endoscopy, initiated 2014-06-25, terminated 2015-01-13. FDA's recall record names no specific 510(k) clearance for this event. Product: Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.. Reason: 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 the peripheral that the cable is connected to..
- Recalling firm
- Karl Storz Endoscopy
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-06-25
- Terminated
- 2015-01-13
- Firm location
- El Segundo, CA, United States
Product description
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
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 the peripheral that the cable is connected to.
Data sourced from openFDA. This site is unofficial and independent of the FDA.