Class II
Medical Device Recall: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F
Howmedica Osteonics Corp. · February 27, 2024
Reason for Recall
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Distribution
Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UK
States Affected
NATIONWIDE
Quantity Affected
0
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1631-2024
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.