Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Specialty Audible Torque Wrench Mfg by: Stryker Spine Recalled by Stryker Spine Due to Stryker has received a complaint from customers relating...
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
Specialty Audible Torque Wrench Mfg by: Stryker Spine, Catalog number IS3002XLP, Non-sterile. Used to final tighten to 12 Nm the blocker of the XIA 3, Hooks, Monoaxial Screws, Rod to Rod Connectors and Off-set connectors.
Quantity: 15 units
Why Was This Recalled?
Stryker has received a complaint from customers relating to a fracture during the use of the Specialty Audible Torque Wrench in surgery.
Where Was This Sold?
This product was distributed to 8 states: GA, IN, MI, NJ, OH, PA, TX, VA
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