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Codman Microsensor Basic Kit Recall

Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is r

Updated December 12, 2025

The Codman Microsensor Basic Kit (Catalog Number 626631US) used for intracranial pressure monitoring may have corrosion stains on the included 14-gauge Tuohy Needle, which could affect the safety and reliability of the monitoring device.

Is the Integra LifeSciences Corp. (NeuroSciences) recalled? Yes. This product was recalled by FDA on December 12, 2025. Details below.

What is recalled

Codman Microsensor Basic Kit, Catalog Number 626631US, manufactured by Integra LifeSciences Corp. (NeuroSciences Division), used for subdural and intraparenchymal intracranial pressure (ICP) monitoring.

Am I affected

You are affected if you have received or are using the Codman Microsensor Basic Kit with Catalog Number 626631US, particularly if it includes the 14-gauge Tuohy Needle component.

What to do right now

Contact Integra LifeSciences Corp. to report your kit and receive instructions for inspection or replacement of the affected component. Do not use the kit if corrosion stains are visible on the needle.

The hazard

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

Brands affected

Integra LifeSciences Corp. (NeuroSciences)
Source
FDA
Category
Baby & Kids
Recall ID
fda-Z-1036-2026
Classification
Class II
Recalled
December 12, 2025
Read the official notice

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