Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
- Recall date
- July 25, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-3131-2024
- FDA classification
- Class II
- Brand / firm
- Technomed Europe
- Sold / distributed
- US: FL, CA, TX, IL, NY, PA, MA
Why it was recalled
Product has have presence of brown discoloration or substance on the hinge area of the device
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
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