Howmedica recalls TRIDENTII PSL Cluster58F hip implants with potential smooth acetabular shell edges. This may cause dislocation in high-risk hip patients. Affected units have specific catalog and lot numbers.
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Howmedica is recalling TRIDENTII PSL Cluster58F hip implants for patients at high risk of hip dislocation. The recall is due to a potential smooth edge on the acetab: this could increase dislocation risk during surgery or recovery.
The acetabular shell may have excessive deburring, creating a smooth surface on the edge. This smooth edge could potentially increase the risk of dislocation during hip surgery or recovery for patients at high risk.
Patients with high risk of hip dislocation who received this specific implant model. Those with the catalog number 742-11-58F and lot number 13927651 are most affected.
Check if your implant has catalog number 742-11-58F and lot number 13927651. This model is intended for primary and revision hip surgeries in high-risk patients.
Verify your implant's catalog number (742-11-58F) and lot number (13927651) to confirm if it's affected.
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge, which could increase dislocation risk for high-risk patients.
Check your implant's catalog number (742-11-58F) and lot number (13927651) to see if it's affected. If so, contact Howmedica for further instructions.
The recall is for potential increased dislocation risk in high-risk patients, but the hazard does not indicate a risk of serious injury in normal use.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-1631-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-1631-2024 from Howmedica. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
