Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: Recalled by Stryker GmbH Due to When creating a correction plan with the Correct...
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 GmbH directly.
Affected Products
Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: HLRF 1.0-2/002, HLRF 1.1-2/002
Quantity: 233
Why Was This Recalled?
When creating a correction plan with the Correct Axial First button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an erroneously accelerated correction plan for the axial portion of the plan.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker GmbH
Stryker GmbH has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report