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

Recall Z-0953-2017 — NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius

U.S. FDA — Device Enforcement · France · 2016-12-19 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0953-2017
Date of alert
2016-12-19
Country / jurisdiction
France
Risk level
Class II
Risk type
recall
Brand
In2Bones, SAS
Product category
device
Product type
Devices
Reported risk: Dimensional non-conformity of the thread on the screw head.
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.