Howmedica recalls TRIDENTII HEMI CLUSTER48D hip implants for potential smooth acetabular shell edges that could cause dislocation in high-risk patients. Affected units include specific catalog numbers and lot ranges.
The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
Howmedica is recalling TRIDENTII HEMI CLUSTER4:8D hip implants for patients at high risk of hip dislocation. The recall is due to a potential smooth edge on the acetabular shell that could increase dislocation risk during surgery.
The acetabular shell may have excessive deburring, creating a smooth surface on the edge. This smooth edge could potentially lead to dislocation during hip surgery for high-risk patients.
Patients who received the TRIDENTII HEMI CLUSTER48D hip implant for primary or revision surgeries at high risk of hip dislocation. Surgeons and medical facilities using this specific implant model are most at risk.
Check for the catalog number 702-11-48D and lot numbers 14875651, 15005253, or 16044255. The implant is intended for primary and revision hip surgeries in high-risk patients.
Verify the catalog number and lot numbers listed in the recall notice to confirm if your implant is affected.
The recall is for specific models that may have a smooth edge on the acetabular shell, which could increase dislocation risk in high-risk patients. Consult your surgeon for current safety.
Check the catalog number and lot numbers provided in the recall notice to determine if your implant is affected. Contact Howmedica for further guidance.
The recall addresses a potential smooth edge that could increase dislocation risk during surgery, but no immediate risks are reported for patients already implanted.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-1622-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-1622-2024 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.
