NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 (Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands) – product has have presence of brown di... (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Brand
Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands
Lot Codes / Batch Numbers
UDI/DI 08718375869659, Lot Numbers: 061158, 061380
Products Sold
UDI/DI 08718375869659, Lot Numbers: 061158, 061380
Technomed Europe Amerikalaan 71 Maastricht-Airport Netherlands is recalling NEUROSIGN Disposable Stimulating Dissector, REF 5888-00 due to Product has have presence of brown discoloration or substance on the hinge area of the device. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product has have presence of brown discoloration or substance on the hinge area of the device
Recommended Action
Per FDA guidance
Technomed Europe issued a FIELD SAFETY NOTICE to its consignees on 07/25/2024 via email. The notice explained the issue, potential risk, and requested the cessation of distribution and quarantine of the affected product pending return of the affected product. Distributors were directed to notify those to whom the product was distributed by forwarding a copy of the notice.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, FL, IL, MA, NY, PA, TX
Page updated: Jan 10, 2026