Howmedica recalls Triathlon Femoral Distal Augments due to overhang issue that may protrude beyond mating component, risking improper fit during knee surgery.
Due to device overhang issue that protrudes beyond the medial periphery of the mating femoral component
Howmedica is recalling Triathlon Femoral Distal Augments (size 2 left) used in knee replacements because they may protrude beyond the mating component. This could lead to improper fit during surgery, potentially causing complications.
The device has an overhang issue that causes it to protrude beyond the medial periphery of the mating femoral component. This could lead to improper fit during knee surgery, potentially causing complications if the components don't align correctly.
Patients who received Triathlon Femoral Distal Augments (size 2 left) for knee replacements are affected. Surgeons using these components during revision Total Knee Arthroplasty (TKA) are most at risk.
Check for Triathlon Femoral Distal Augments (15mm, size 2 left) used with Triathlon TS Femoral Components during revision knee surgery. Products were sold with expiration dates up to June 30, 2024, and include specific lot numbers listed in the recall.
Identify if your Triathlon Femoral Distal Augment (15mm, size 2 left) has an expiration date on or before June 30, 2024, and matches the listed lot numbers.
The device has an overhang issue that causes it to protrude beyond the medial periphery of the mating femoral component, which could lead to improper fit during knee surgery.
No, but you should check if your implant matches the recall criteria and contact Howmedica if you have concerns.
The recall record does not specify a remedy, so you should contact Howmedica directly for guidance.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2759-2019 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2759-2019 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.
