HomeMedical Device recalls
Medium severity

Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is required. The kit is indicated for use in both subdural and intraparenchymal pressure monitoring applications only.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateDecember 12, 2025
ReportedJanuary 14, 2026
Recalling firmIntegra LifeSciences Corp. (NeuroSciences)
Country / regionUnited States NJ

Hazard

Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

Affected products

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