Howmedica recalls Triathlon Femoral Distal Augments with overhang issue that may protrude beyond mating component. Affected units include specific catalog numbers and lots. Contact for remedy.
Due to device overhang issue that protrudes beyond the medial periphery of the mating femoral component
Howmedica is recalling Triathlon Femoral Distal Augments that have a design flaw causing them to protrude beyond the mating femoral component. This could lead to improper joint alignment during knee 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 alignment during knee surgery, potentially causing joint instability or complications.
Orthopedic surgeons and patients undergoing total knee arthroplasty (TKA) who use the recalled Triathlon Femoral Distal Augments. Surgeons using the specific catalog numbers and lots listed are most at risk.
Check for the product name 'Triathlon Femoral Distal Augment 15MM - Size 2 Right' with catalog number 5542-A-202. Affected lots have expiration dates on or before June 30, 2024, and include specific lot numbers listed in the recall.
Verify the catalog number and lot numbers listed in the recall to confirm if your device is affected.
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 alignment during knee surgery.
Affected lots include specific numbers listed in the recall, all with expiration dates on or before June 30, 2024.
The recall does not specify a remedy, so no action is required beyond checking if your device is affected.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2760-2019 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2760-2019 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.
