Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine Manufactured Recalled by Stryker Spine Due to Reported jamming of the impaction handle when assembled...
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 Aero-AL Impaction handle Catalog Number 48921007. Stryker Spine Manufactured by : Stryker Spine SAS France Used to facilitate insertion of the Aero-AL cage into the disc space.
Quantity: 31 units
Why Was This Recalled?
Reported jamming of the impaction handle when assembled to the Inserter guide at the threads.
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