Howmedica recalls UNITRAX 38mm hip implant components due to potential size mismatch between packaging labels and actual devices. Affected units include specific catalog numbers and lot numbers. Consumers should contact Howmedica for details.
Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis Head Component potentially may not match the device within the packaging. This product mix only involves the three (3) sizes (43mm, 42mm, and the 38mm)
Howmedica is recalling UNITRAX 38mm hip implant components because the size on the package label might not match the actual device. This mismatch could lead to improper fitting during surgery, which is critical for hip replacements.
The implant component's size on the packaging label might not match the actual device. This mismatch could cause improper fitting during hip replacement surgery, potentially leading to complications.
Patients who received a UNITRAX 38mm hip implant component during surgery are affected. Surgeons and medical facilities that used these components are at higher risk.
Check for catalog number 6942-5-038 and lot numbers JT38AD or E94VEV on the packaging. This product was sold with specific sizes (43mm, 42mm, and 38mm).
Reach out to Howmedica Osteonics Corp. for specific guidance on affected units and next steps.
The recalled implant is the UNITRAX 38mm Endoprosthesis Head Component.
Check for catalog number 6942-5-038 and lot numbers JT38AD or E94VEV on the packaging.
The recall does not specify a fix; affected users should contact Howmedica for details.
We’ve drafted a message you can send Howmedica to request your refund or repair — edit it as you like.
Subject: Recall Z-2372-2024 — Howmedica Howmedica Hello, I own a Howmedica that is covered by recall Z-2372-2024 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.
