Class II
Medical Device Recall: NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Technomed Europe · July 25, 2024
Reason for Recall
Product has have presence of brown discoloration or substance on the hinge area of the device
Distribution
US: FL, CA, TX, IL, NY, PA, MA
States Affected
CA, FL, IL, MA, NY, PA, TX
Quantity Affected
71 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3131-2024
Status: ongoing
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