Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners failed the oxidation testing performed prior...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact OMNIlife science Inc. directly.
Affected Products
OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code: H6-25328
Quantity: 14 units
Why Was This Recalled?
Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About OMNIlife science Inc.
OMNIlife science Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report