PlainRecalls
FDA Devices Moderate Class II Ongoing

NEUROSIGN Disposable Stimulating Dissector, REF 5888-00

Reported: September 18, 2024 Initiated: July 25, 2024 #Z-3131-2024

Product Description

NEUROSIGN Disposable Stimulating Dissector, REF 5888-00

Reason for Recall

Product has have presence of brown discoloration or substance on the hinge area of the device

Details

Recalling Firm
Technomed Europe
Units Affected
71 units
Distribution
US: FL, CA, TX, IL, NY, PA, MA
Location
Maastricht-Airport

Frequently Asked Questions

What product was recalled?
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00. Recalled by Technomed Europe. Units affected: 71 units.
Why was this product recalled?
Product has have presence of brown discoloration or substance on the hinge area of the device
Which agency issued this recall?
This recall was issued by the FDA Devices on September 18, 2024. Severity: Moderate. Recall number: Z-3131-2024.