Howmedica recalls Series II Tibial Bear Insert (part 3052-0524) manufactured over 5 years ago due to potential oxidation in UHMWPE material. Affected units may have reduced durability.
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 Series II Tibial Bear Inserts (part number 3052-052:0524) that were manufactured more than 5 years ago. These inserts could have elevated oxidation in the UHMWPE material, which might affect their durability and performance in knee replacements.
The insert uses UHMWPE material that can oxidize over time. Oxidation may weaken the material, potentially reducing its durability and performance in knee replacements. However, this does not cause immediate injury or failure.
Patients who received this specific knee replacement insert from Howmedica over 5 years ago. Those with the part number 3052-0524 are most at risk.
Check if your knee replacement insert has the part number 3052-0524 and was manufactured more than 5 years ago. Lot number K349TP is also associated with this recall.
Verify your insert's part number is 3052-0524 and it was manufactured more than 5 years ago.
No, the recall does not require immediate discontinuation. The product may still be safe for use if it's within the 5-year timeframe.
The recall does not specify a remedy, so no action is required unless you want to check for potential issues.
The recall indicates a potential durability issue but does not mention immediate injury risks, so it's considered low risk.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-0874-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-0874-2024 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.
