FDA Device recall Z-3131-2024
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
- FDA Device
- Class II
- ongoing
- Published 2024-09-18
On 2024-09-18 the FDA classified a Class II recall of NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 by Technomed Europe, citing product has have presence of brown discoloration or substance on the hinge area of the device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3131-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-25 |
| Published | 2024-09-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Technomed Europe |
| Distribution | CA, FL, IL, MA, NY, PA, TX |
Product
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Reason
Product has have presence of brown discoloration or substance on the hinge area of the device
Identifiers
| code_info | UDI/DI 08718375869659, Lot Numbers: 061158, 061380 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3131-2024%22
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