Class II

Medical Device Recall: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants.

Onkos Surgical, Inc. · July 11, 2025

Reason for Recall

Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.

Distribution

US Nationwide distribution in the states of AK, AZ, CA, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NY, OH, TN, TX, UT, WA & WI.

States Affected

NATIONWIDE

Quantity Affected

15 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2424-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Onkos Surgical, Inc. Medical Device Recall: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING STRAIGHT SLOTTED SPLINED 2/3 PLASMA. Canal filling stem implants. | SafeCheck