Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LITe Decompression Snake Arm Recalled by Stryker Spine Due to Product arm was manufactured with the incorrect clamp...
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
LITe Decompression Snake Arm, REF 48080230
Quantity: 9
Why Was This Recalled?
Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.
Where Was This Sold?
This product was distributed to 4 states: MD, MI, NM, TX
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