Howmedica Osteonics recalls SCORPIO TS TIB INSERT knee replacement implants with UHMWPE material over 5 years old due to potential oxidation. Affected units have specific part numbers and lot 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 Osteonics is recalling SCORPIO TS TIB INSERT knee replacement implants that were manufactured with UHMWPE material more than 5 years ago. This could lead to material degradation over time, though the risk is not immediate.
The UHMWPE material in the implant can oxidize over time, especially after 5 years of use. Oxidation weakens the material, potentially affecting its performance in the joint. However, this does not cause immediate harm or failure.
Knee replacement surgery patients who received the SCORPIO TS TIB INSERT implant with part number 72-4-7514 and lot numbers 482LM8 or HH43K7. Patients with implants older than 5 years since manufacturing are most at risk.
Check for part number 72-4-7514 and lot numbers 482LM8 or HH43K7 on the implant. The product was sold with a specific GTIN: 07613327034820.
Look for part number 72-4-7514 and lot numbers 482LM8 or HH43K7 on the implant.
The recall does not require immediate discontinuation. The risk is related to material degradation over time, not an immediate hazard.
Check the implant details for part number 72-4-7514 and lot numbers 482LM8 or HH43K7. If affected, contact Howmedica Osteonics for further instructions.
The recall states potential material degradation but does not mention a risk of serious injury. The hazard is not immediate.
We’ve drafted a message you can send Howmedica Osteonics to request your refund or repair — edit it as you like.
Subject: Recall Z-0878-2024 — Howmedica Osteonics Howmedica Osteonics Hello, I own a Howmedica Osteonics that is covered by recall Z-0878-2024 from Howmedica Osteonics. 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.
