Howmedica recalls TRIDENTII HEMI CLUSTER44B hip implants for potential smooth acetabular shell edges that could cause dislocation in high-risk 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 HEMI CLUSTER4:44B hip implants that may have a smooth edge on the acetabular shell. This could increase the risk of hip dislocation in patients with high risk of dislocation. Affected patients should contact the manufacturer for details.
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.
Patients who received this specific hip implant model for high-risk hip dislocation cases. Those with the catalog number 702-11-44B and lot number 14974852 are most at risk.
Check for the catalog number 702-11-44B and lot number 14974852 on the implant packaging. This model is indicated for primary and revision patients at high risk of hip dislocation.
Look for catalog number 702-11-44B and lot number 14974852 on the implant packaging.
The recall indicates a potential risk of smooth acetabular shell edges that could increase dislocation risk in high-risk patients. The manufacturer recommends checking if you have the specific catalog and lot numbers.
Contact Howmedica Osteonics Corp. directly to confirm if your implant is affected and get instructions.
Check for catalog number 702-11-44B and lot number 14974852 on the implant packaging. This model is indicated for high-risk hip dislocation cases.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-1621-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-1621-2024 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.
