Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker Spine Due to There were two potential interference conditions identified with...
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
AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device system that uses hydraulic pressure to expand the implant in-situ. The purpose of the AccuLIF PL Tubing Set (cat#900301) and AccuLIF TL Tubing Set (cat#905103) is to deliver pressurized saline from a syringe to the AccuLIF implant for in-situ expansion. The Tubing Set attaches to the AccuLIF Insertion handle at two district locations: the "junction block" and the "manifold." The PL and TL Tubing Sets are Class 2 instruments not intended to sustain or support life.
Quantity: 413 units
Why Was This Recalled?
There were two potential interference conditions identified with the way the tubing set attaches to the inserter.
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