FDAFDA · Food and drugs·Recall number Z-3131-2024
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Published September 18, 2024 · Recall initiated: July 25, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Product has have presence of brown discoloration or substance on the hinge area of the device
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Technomed Europe
- Distributor
- US: FL, CA, TX, IL, NY, PA, MA
- Lot
- UDI/DI 08718375869659, Lot Numbers: 061158, 061380
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Netherlands
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