Class II
Medical Device Recall: X3 TRIATHLON CS INSERT NO 6 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
143 units (US)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1260-2024
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.