Medium risk Baby & KidsClass II

Integra LifeSciences Corp. (NeuroSciences) 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

Integra LifeSciences Corp. (NeuroSciences) is recalling Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the CODMAN MICROSENSOR Basic Kit is indicated when direct ICP monitoring is r. Hazard: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.

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. 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.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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

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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