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

Recall Z-2791-2016 — Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System is intended to provide strong and stable internal fixation with minimal soft tissue irritation of the distal femur. (1( Open and closed femoral fractures, (2) Pseudoarthrosis and correction osteotomy, (3) Pathologic fractures, impen

U.S. FDA — Device Enforcement · United States · 2016-06-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2791-2016
Date of alert: 2016-06-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Howmedica Osteonics Corp.
Product category: device
Product type: Devices

Reported risk: Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled and distributed to the field.

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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