Integra NeuroSciences recalls Codman CereLink ICP Sensor Basic Kit (Catalog 826850) due to potential corrosion stains on the 14-gauge Tuohy needle. This may affect medical use in intracranial pressure monitoring.
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
Integra NeuroSciences is recalling Codman CereLink ICP Sensor Basic Kit (Catalog Number 826850) because the 14-gauge Tuohy needle may have corrosion stains. This could impact the accuracy of intracranial pressure monitoring during medical procedures.
The 14-gauge Tuohy needle in the kit may develop corrosion stains. While this could potentially affect the accuracy of pressure readings during medical procedures, the recall does not indicate a risk of injury or serious harm.
Patients undergoing intracranial pressure monitoring procedures who use the Codman CereLink ICP Sensor Basic Kit with the specified lot numbers. Medical professionals using this kit for subdural or intraparenchymal pressure monitoring are most at risk.
Check if your kit has Catalog Number 826850 and lot numbers listed in the recall (e.g., 7261958, 7266691, etc.). The kit includes the CereLink ICP Sensor and a 14-gauge Tuohy needle with stylet.
Verify your kit's catalog number (826850) and lot numbers from the list provided in the recall.
The recall states potential corrosion stains on the needle, but does not indicate a risk of injury or serious harm. This is considered a low-risk issue.
The recall does not specify a remedy, so no action is required beyond checking if your kit matches the catalog and lot numbers listed.
Check if your kit has Catalog Number 826850 and one of the listed lot numbers (e.g., 7261958, 7266691, etc.).
We’ve drafted a message you can send Integra NeuroSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1037-2026 — Integra NeuroSciences Integra NeuroSciences Hello, I own a Integra NeuroSciences that is covered by recall Z-1037-2026 from Integra NeuroSciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
