Howmedica recalls P7 28MM 10 DEGREE +4MM knee replacement inserts made over 5 years ago due to potential oxidation in UHMWPE material. Affected units have specific lot numbers and part numbers.
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 knee replacement inserts that were manufactured more than 5 years ago because the material may oxidize over time. This could affect the insert's performance and safety in the body.
The insert is made from UHMWPE (a type of plastic) that can oxidize over time. Oxidation may weaken the material, potentially causing it to fail during use in the knee joint.
Patients who received this specific knee replacement insert model (P7 28MM 10 DEGREE +4MM) from Howmedica. Those with implants made more than 5 years ago are most at risk.
Check for the part number 6302-6-107 and lot numbers 61311701 or 62122001 on the insert. This product was sold as a knee replacement implant.
Look for the part number 6302-6-107 and lot numbers 61311701 or 62122001 on the insert.
The product was manufactured using UHMWPE raw material over 5 years of age, which has the potential for elevated oxidation levels that could impact material properties.
The recall does not specify a remedy, so no action is required beyond checking if your insert matches the described part numbers and lot numbers.
Check for the part number 6302-6-107 and lot numbers 61311701 or 62122001 on the insert.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-0904-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-0904-2024 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.
