NEUROSIGN Disposable Stimulating Dissector recall
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Why was NEUROSIGN Disposable Stimulating Dissector recalled?
Product has have presence of brown discoloration or substance on the hinge area of the device
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 08718375869659, Lot Numbers: 061158, 061380
- Product
- NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
- Recalling firm
- Technomed Europe
- Quantity
- 71 units
- Distribution
- US: FL, CA, TX, IL, NY, PA, MA
- Recall date
- September 18, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)