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

Recall Z-2456-2015 — Concave Reamer Head, 16 mm; Concave Reamer Head, 18 mm; Concave Reamer Head, 20 mm; Concave Reamer Head 22 mm; Convex Reamer Head, 16 mm; Convex Reamer Head, 18 mm; Convex Reamer Head 20 mm; Convex Reamer Head 22 mm, used with Gridlock Plating system, for use in trauma and reconstructive procedures

U.S. FDA — Device Enforcement · United States · 2015-07-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2456-2015
Date of alert
2015-07-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Trilliant Surgical Ltd.
Product category
device
Product type
Devices
Reported risk: The cannulation of the Concave and Convex Reamer Heads may be too small to allow the Guide Pin to freely pass through.
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.

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