NEUROSIGN Disposable Stimulating Dissector — Class II medical device recall Z-3131-2024
Ongoing recall by Technomed Europe, reported 2024-09-18, distributed in CA, FL, IL, MA, NY, PA, TX. Product has have presence of brown discoloration or substance on the hinge area of the device
| Recall number | Z-3131-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Technomed Europe, Maastricht-Airport, Netherlands |
| Recall initiated | 2024-07-25 |
| Classified | 2024-09-12 |
| Reported by FDA | 2024-09-18 |
| Distributed | CA, FL, IL, MA, NY, PA, TX |
| Quantity | 71 units |
| UPC / GTIN / UDI-DI | 08718375869659 |
| Lot numbers | 061158, 061380 |
| Model numbers | 5888-00 |
Product
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Reason for recall
Product has have presence of brown discoloration or substance on the hinge area of the device
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3131-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.