FDA Device recall Z-2570-2018
XLTEK EMU40EX EEG Headbox
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of XLTEK EMU40EX EEG Headbox by Natus Neurology, citing possible degradation of an internal electronic component over time which may cause the XLTEK EMU 40EX Breakout box to fail. It may feel hot and plastic case may start melting.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2570-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-05-15 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Natus Neurology |
| Distribution | AL, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NV, NY, OH, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI |
Product
XLTEK EMU40EX EEG Headbox
Reason
Possible degradation of an internal electronic component over time which may cause the XLTEK EMU 40EX Breakout box to fail. It may feel hot and plastic case may start melting.
Identifiers
| code_info | Part Numbers: 10406, 002933 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2570-2018%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.