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CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) M

FDA device recall Z-0548-2024 · posted 2023-12-14 · Open, Classified

Recall details

Recalling firm
Integra LifeSciences Corp.
Reason for recall
Firm is expanding the existing recall RES 90457 for the Cerelink, initiated in June 2022, to include all CereLink ICP Extension Cables. The updated corrective action includes a design change to the extension cable to address the "out of range readings" issue.
Action taken
On October 5, 2023, the firm issued an updated letter, intended to replace the notification sent on June 22, 2022 for the out-of-range readings issue (RES 90457). As an output of the root cause and failure investigation, the design of the extension cable is being modified to incorporate a solution to address the "out of range readings" issue. The firm instructed customers to return all existing CereLink ICP Extension Cables in their inventory. This includes all CereLink ICP Extension Cables included with the monitor AND all CereLink ICP Extension Cables provided separately. Customers should check their inventory and quarantine any affected product. Once the firm receives the customer's response form, the firm will provide instructions to return the product. Customers with questions about this recall should contact their Account Manager.
Root cause
Device Design
Status
Open, Classified
Product code
GWM
Quantity affected
4941
Distribution
US distribution nationwide to the following states: AL AR AZ CA CO CT DC DE FL GA IA KY LA MA ME MN ND NE NH NJ NY OK PA RI TN TX UT VA WI WV OUS distribution to Australia/New Zealand, Canada, and Eur
Date initiated
2023-10-05
Date posted
2023-12-14
Location
Princeton, NJ

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Related 510(k) clearances

RecordFirmDate
CereLink ICP Monitor (826820), CereLink ICP Extension Cable (826845) (K232890)Integra Lifesciences Production Corporation2024-02-04
CereLink ICP Monitor (K210993)Integra Lifesciences Production Corporation2021-04-30