Class II — Technomed Europe
| Recalling firm | Technomed Europe |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Product has have presence of brown discoloration or substance on the hinge area of the device |
| Product | NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 |
| Quantity | 71 units |
| Distribution | US: FL, CA, TX, IL, NY, PA, MA |
| Initiated | 2024-07-25 |
| Classified | 2024-09-12 |
| Recall number | Z-3131-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Technomed Europe (Z-3131-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95188/
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