FDANovember 7, 2019device
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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
What to do
FDA enforcement status: Terminated
Brands named
howmedica osteonicshowmedica
UPCs
04546540035806
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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