Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for Recalled by Howmedica Osteonics Corp. Due to May have a missing locking wire causing delay...
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 Howmedica Osteonics Corp. directly.
Affected Products
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Quantity: 20 units
Why Was This Recalled?
May have a missing locking wire causing delay in surgery while retrieving a back-up device or implantation of a device that is missing a locking wire
Where Was This Sold?
This product was distributed to 9 states: CA, FL, GA, IA, MA, MI, NC, OH, WI
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report