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Howmedica Osteonics Corp. recalls Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepar
Recalled January 22, 2020 · FDA recall Z-0811-2020 · Howmedica Osteonics
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 · FDA Class II
Units
20 units
Sold at
CA, FL, GA , IA, MA, MI, NC, OH, WI Foreign: Canada, Japan
Description
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
Product
Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for cementless and/or cemented fixation within the prepared acetabulum Catalog #: 2041C-3254
Manufacturer(s)
Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →