Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to Unidentified substance of unknown impact was identified on...
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 Onkos Surgical, Inc. directly.
Affected Products
ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.
Quantity: 15 units
Why Was This Recalled?
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Onkos Surgical, Inc.
Onkos Surgical, Inc. has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report