Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Integra LifeSciences Corp. to request your refund or repair — edit it as you like.
Subject: Recall Z-0978-2025 — Integra LifeSciences Corp. Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Hello, I own a Integra LifeSciences Corp. recalls CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL. Implantable device that provides that is covered by recall Z-0978-2025 from Integra LifeSciences Corp.. 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.
