OMNIlife science recalls ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28 due to potential higher wear rate leading to revision surgery.
Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.
OMNIlife science is recalling a specific hip prosthesis component because it may wear out faster than expected, which could require surgery. This affects patients who have received this particular implant.
The acetabular liners failed oxidation testing before release, which means they may wear down faster than intended. This increased wear rate could lead to the need for revision surgery to replace the implant.
Patients who received the ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28 during surgery are affected. Those with this specific implant are at risk of needing revision surgery.
Check for the product code H6-25128 and lot number 31740 on the implant. This specific hip prosthesis component was sold by OMNIlife science.
Look for product code H6-25128 and lot number 31740 on the implant.
The acetabular liners failed oxidation testing before release, which may cause a higher wear rate leading to revision surgery.
Check for product code H6-25128 and lot number 31740 on the implant. If you have this specific implant, contact OMNIlife science for further instructions.
The recall states a higher wear rate could lead to revision surgery, but there is no mention of immediate injury risks.
We’ve drafted a message you can send OMNIlife science to request your refund or repair — edit it as you like.
Subject: Recall Z-2480-2019 — OMNIlife science OMNIlife science Hello, I own a OMNIlife science that is covered by recall Z-2480-2019 from OMNIlife science. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
