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

Recall Z-1637-2014 — TRIGEN INTERTAN 1.5 NAIL: (1) REF 71676515, 10 MM X 10 CM, 125 degree, LEFT, (2) REF 71676556, 11.5 MM X 36 CM, 125 degree, RIGHT, (3) REF 71676558, 11.5 MM X 38 CM, 125 degree, RIGHT, (4) REF 71676561, 11.5 MM X 42 CM, 125 degree, LEFT, Smith & Nephew, Inc. Orthopedic fixation devic

U.S. FDA — Device Enforcement · United States · 2014-04-04 · 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-1637-2014
Date of alert: 2014-04-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Smith & Nephew Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 71676515

Reported risk: A manufacturing error resulted in the set screw being inserted too deep in the affected nails.

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.

Related