ClearanceBrief
Recall Z-0977-2025 ยท JXG Shunt, Central Nervous System And Components

Integra LifeSciences Corp.

CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.

DateJan 17, 2025 (initiated Dec 16, 2024)
StatusOpen, Classified
ReasonPotential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
Root causeLabeling Change Control
ActionIntegra LifeSciences notified consignees on about 12/16/2024 via letter. Consignees were instructed to review and understand the information provided in the letter, complete and return the provided Customer Acknowledgement Form, remove any affected units from service and quarantine them, arrange for return of affected units, and forward the notification to anyone who utilizes the affected units. Distributors were instructed to follow the same directions but also requested to notify any customers if product was further distributed, and return affected units.
Quantity132 units
DistributionUS Nationwide distribution in the states of FL, NC, MA, MN, OH, DC, VA, CA, WI, NE, TX, NY, MI, OR, NJ, SC, AZ, UT, RI, IN, GA, CO and the countries of Canada, Australia, New Zealand, Cyprus, Sweden, Finland, Slovenia and Great Britain.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.