---
title: "NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 — FDA record Z-3131-2024 | Is It on Recall"
description: "Product has have presence of brown discoloration or substance on the hinge area of the device"
url: https://isitonrecall.com/recall/fda-device-z-3131-2024-neurosign-disposable-stimulating-dissector-ref-5888-00/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 — FDA record Z-3131-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 25, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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
- **Classification**: Class II
- **Recalling firm**: Technomed Europe
- **Quantity**: 71 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3131-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3131-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 08718375869659, Lot Numbers: 061158, 061380 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: FL, CA, TX, IL, NY, PA, MA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Sep 18, 2024
- **Recall initiation date**: Jul 25, 2024
- **Center classification date**: Sep 12, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3131-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Technomed Europe records](https://isitonrecall.com/brand/technomed-europe/)