Howmedica recalls SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 knee replacement parts manufactured over 5 years ago due to potential oxidation in UHM:PE material.
Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.
Howmedica is recalling SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 knee replacement parts made more than 5 years ago because oxidation in the UHMWPE material could affect its properties. This recall affects patients who have received this specific knee replacement part.
The UHMWPE material in the knee replacement part can oxidize over time, especially after 5 years. Oxidation may weaken the material, potentially affecting the part's performance and longevity.
Patients who received the SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 knee replacement part from Howmedica. Those with the part manufactured over 5 years ago are most at risk.
Check if your knee replacement part has the model name 'SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7' and part number 73-2710. Look for lot numbers V25H, MD9E, 5MYL, H9T8, or 845P.
Identify if your knee replacement part matches the model name 'SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7' and part number 73-2710.
The UHMWPE material in the knee replacement part can oxidize over time, especially after 5 years, which may affect its material properties.
Check if your knee replacement part matches the model name and part number listed in the recall. If it does, contact Howmedica for further instructions.
Look for lot numbers V25H, MD9E, 5MYL, H9T8, or 845P on the part. Also, check for the model name 'SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7' and part number 73-2710.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-0891-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-0891-2024 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.
