Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0863-2014 — Codman Certas Programmable Valve In Line Valve with Siphonguard, Unitized Catheter and Accessories Product Code: 82-8806 Product Usage: The CODMAN CERTAS Programmable Valve is an implantable device that provides constant intraventricular pressure and drainage of CSF (cerebrospinal fluid) for

U.S. FDA — Device Enforcement · United States · 2013-05-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0863-2014
Date of alert: 2013-05-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Codman & Shurtleff, Inc.
Product category: device
Product type: Devices

Reported risk: Codman Certas Programmable Valves used for hydrocephalus may not operate properly

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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