Technomed Europe: Device Recall
Recall #Z-3131-2024 · 07/25/2024
Class II: Risk
Recall Details
- Recall Number
- Z-3131-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Technomed Europe
- Status
- Ongoing
- Date Initiated
- 07/25/2024
- Location
- Maastricht-Airport, Netherlands
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 71 units
Reason for Recall
Product has have presence of brown discoloration or substance on the hinge area of the device
Product Description
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Distribution Pattern
US: FL, CA, TX, IL, NY, PA, MA
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.