CLASS II ONGOING Device recall · Reported 18 Sep 2024 · FDA Enforcement Report
Neurosign Disposable Stimulating Dissector recalled by Technomed Europe
Technomed Europe is recalling Neurosign Disposable Stimulating Dissector, distributed in 7 states. The recall was initiated on 25 Jul 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-3131-2024
- FDA event ID
- 95188
- Recalling firm
- Technomed Europe, Maastricht-Airport
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 25 Jul 2024
- FDA classified
- 12 Sep 2024
- Reported
- 18 Sep 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 25 Jul 2024 | Recall initiated by company | |
| 12 Sep 2024 | Classified by FDA | +49 days |
| 18 Sep 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product has have presence of brown discoloration or substance on the hinge area of the device
Product as listed by the FDA
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Where it was distributed
US: FL, CA, TX, IL, NY, PA, MA
CaliforniaFloridaIllinoisMassachusettsNew YorkPennsylvaniaTexas
Questions about this recall
Why was it recalled?
Product has have presence of brown discoloration or substance on the hinge area of the device
Which lots are affected?
UDI/DI 08718375869659, Lot Numbers: 061158, 061380
Where was it sold?
US: FL, CA, TX, IL, NY, PA, MA
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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