Biomet recalls G7 Acetabular System Dual Mobility Liner (40mm Size D) due to incorrect size labeling. This mismatch may cause improper fit and complications during hip replacement surgery.
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Biomet is recalling a specific hip implant liner because it's labeled as 40mm Size D but is actually 38mm Size C. This size mismatch could lead to improper fit during hip replacement surgery, potentially causing complications.
The liner is labeled as 40mm Size D but is actually 38mm Size C. This size mismatch could cause improper fit during hip replacement surgery, potentially leading to complications like instability or improper joint alignment.
Patients who received this specific hip implant liner during surgery are affected. Surgeons and medical teams using this model during procedures are most at risk.
Check for the model number 110024462 on the outer packaging. The liner is part of the G7 Acetabular System with a 40mm Size D label but is actually 38mm Size C.
Verify the model number on the packaging is 110024462 and the size label matches the actual liner size.
The recall is for a size mismatch that could cause improper fit during hip replacement surgery, but the hazard level is low risk as it only affects specific surgical implants.
Check for the model number 110024462 on the outer packaging. The liner is labeled as 40mm Size D but is actually 38mm Size C.
The recall does not specify a remedy, so contact Biomet directly for guidance on next steps.
We’ve drafted a message you can send Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1284-2023 — Biomet Biomet Hello, I own a Biomet that is covered by recall Z-1284-2023 from Biomet. 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.
