Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision Recalled by Howmedica Osteonics Corp. Due to The acetabular shell may have excessive deburring, resulting...
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 Howmedica Osteonics Corp. directly.
Affected Products
TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D
Quantity: 0
Why Was This Recalled?
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report