Howmedica Osteonics recalls TRIDENTII HEMI CLUSTER52E hip implants for potential smooth acetabular shell edge, which may cause dislocation in high-risk patients. Affected units include specific catalog numbers and lot dates.
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Howmedica Osteonics is recalling TRIDENT: HEMI CLUSTER52E hip implants for patients at high risk of hip dislocation. The recall is due to a possible smooth edge on the acetabular shell that could increase dislocation risk during surgery or after implantation.
The acetabular shell may have excessive deburring, creating a smooth surface on the edge. This smooth edge could potentially lead to dislocation in patients who are at high risk of hip dislocation, especially during surgical procedures or after implantation.
Patients who received the TRIDENTII HEMI CLUSTER52E hip implant for primary or revision surgeries at high risk of hip dislocation. Those with the specific catalog number 702-11-52E and lot numbers 14875852 or 14875853 are most at risk.
Check for the catalog number 702-11-52E and lot numbers 14875852 or 14875853 on the implant packaging or documentation. The product is indicated for use in primary and revision hip surgeries for high-risk patients.
Reach out to Howmedica Osteonics directly to confirm if your implant is affected and get guidance on next steps.
No, this recall specifically applies to TRIDENTII HEMI CLUSTER52E implants with catalog number 702-11-52E and lot numbers 14875852 or 14875853.
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge, which could increase dislocation risk in high-risk patients.
Contact Howmedica Osteonics directly to determine if your implant is affected and to receive further instructions.
We’ve drafted a message you can send Howmedica Osteonics to request your refund or repair — edit it as you like.
Subject: Recall Z-1624-2024 — Howmedica Osteonics Howmedica Osteonics Hello, I own a Howmedica Osteonics that is covered by recall Z-1624-2024 from Howmedica Osteonics. 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.
