FDA Device recall Z-2039-2014
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit by Karl Storz Endoscopy, citing 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 cessa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2039-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-25 |
| Published | 2014-07-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Karl Storz Endoscopy |
| Distribution | US |
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.
Identifiers
| code_info | Serial Numbers: 20110322-01 HLS-20110706-01 HLS-20110315-03 MLS-20101208-01 MLS-20101101-01 MLS-20130418-22 ML…Serial Numbers: 20110322-01 HLS-20110706-01 HLS-20110315-03 MLS-20101208-01 MLS-20101101-01 MLS-20130418-22 MLS-20130715-03 MLS-20130514-06 MLS-20130514-13 MLS-20130514-14 MLS-20130514-09 MLS-20130514-18 MLS-20130514-19 MLS-20130514-16 MLS-20130514-11 MLS-20130514-08 MLS-20130514-15 MLS-20130514-17 HLS-20130523-02 HLS-20130523-04 MLS-20130514-07 HLS-20130523-03 MLS-20130715-04 MLS-20130514-12 MLS-20130514-10 MLS-20110609-01 MLS-20110603-02 MLS-20110603-01 MLS-20110527-02 MLS-20110531-01 MLS-20110531-02 MLS-20110601-01 MLS-20110601-03 MLS-20140411-01 MLS-20130418-18 MLS-20130418-13 HLS16-20130128-04 HLS16-20130128-03 HLS16-20130128-01 HLS16-20130128-02 MLS-20140424-02 MLS-20130514-02 MLS-20130418-21 MLS-20120924-03 LLS-20111003-03 MLS-20111011-03 MLS-20110920-03 MLS-20120117-14 MLS-20120523-03 MLS-20120905-02 LLS-20121112-04 MLS-20130322-01 MLS-20120713-05 MLS-20110713-04 MLS-20110629-01 MLS16-20131028-01 MLS-20120208-01 HLS24- |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2039-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.