Howmedica recalls SCORPIO recessed patella knee implants (part 3044-0032) with lot numbers 6LR4, R14V, N882 due to potential oxidation in older UHMWPE 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 certain SCORPIO recessed patella knee implants that were manufactured over 5 years ago. These implants may have elevated oxidation levels in the UHMWPE material, which could affect their long-term performance.
The UHMWPE material in these implants can oxidize over time, especially after 5 years of use. Oxidation may weaken the material, potentially affecting the implant's long-term performance and stability.
Patients who received the SCOR: 3044-0032 knee implant with lot numbers 6LR4, R14V, or N882. Those with implants older than 5 years are most at risk.
Check the product label for part number 3044-0032 and lot numbers 6LR4, R14V, or N882. These implants were sold with GTIN 07613327033823.
Look for part number 3044-0032 and lot numbers 6LR4, R14V, or N882 on the implant.
The UHMWPE material in these implants may oxidize over time, especially after 5 years of use, which could affect long-term performance.
Check the product label for part number 3044-0032 and lot numbers 6LR4, R14V, or N882. If you have these, contact Howmedica for further instructions.
The recall is for potential long-term performance issues, not immediate injury risks. The hazard is described as oxidation affecting material properties over time.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-0872-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-0872-2024 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.
