Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Recalled by Stryker Spine Due to Beginning in February 2011, Stryker Spine began receiving...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Spine directly.
Affected Products
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 Use: The trials are designed and intended to measure the height of the disc space intra-operatively.
Quantity: 273 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Spine
Stryker Spine has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report