Class II

Medical Device Recall: X3 TRIATHLON CS INSERT NO 3 10 MM

Howmedica Osteonics Corp. · February 6, 2024

Reason for Recall

Potential packaging breaches of inner blister and outer sterile blister.

Distribution

Domestic: Nationwide Distribution; Foreign: Australia, Canada, Chile, Colombia, Korea, & Japan.

States Affected

NATIONWIDE

Quantity Affected

132 units (US); 26 units (OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1259-2024

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.

Howmedica Osteonics Corp. Medical Device Recall: X3 TRIATHLON CS INSERT NO 3 10 MM | SafeCheck