Reported Jan 29, 2025 · Ongoing
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL. Implantable device that provides…
Integra LifeSciences Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Integra LifeSciences Corp. · 1100 Campus Rd · Princeton, NJ · 08540-6650
Is this the product you have?
- CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only
- Model Number828810PL. Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus
- Lot codes and dates
- UDI-DI10381780535881
- Lot Numbers
74167907432471743492974349307438312 and 7438313
- Amount recalled
- 170 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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