Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due to The device may have improper screw hole placement...
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
APEX INTERFACE Hemi 54X and Flared 56X, 3 Hole Acetabular Shells; Model: H5-12354, H5-11356. Product Usage: The Apex Interface Acetabular System is intended for use in combination with the Apex Modular Hip Stem in total hip replacement procedures.
Quantity: 112
Why Was This Recalled?
The device may have improper screw hole placement due to inaccurate location of the index line.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Omnilife Science Inc.
Omnilife Science Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report