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

Recall Z-2033-2012 — Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Z.1 Marticot-33610-Cestas -France +33 (0) 5.57.97.06.30 http;//www.stryker.com Distributed in the USA by Stryker Spine 2 Pearl Court. Allendale NJ 07401-1677 USA +1-201-780-8000 Cestas France 33610. Intended Us

U.S. FDA — Device Enforcement · United States · 2012-01-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2033-2012
Date of alert: 2012-01-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Spine
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 48392206

Reported risk: Beginning in February 2011, Stryker Spine began receiving reports related to the shaft of the AVS Navigator trial failing at the junction of the trial head.

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

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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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