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Stryker Howmedica Osteonics Corp. recalls Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
Recalled March 20, 2013 · FDA recall Z-0919-2013 · Stryker Howmedica Osteonics
Hazard
Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use. · FDA Class II
Units
48 units
Sold at
Nationwide Distribution.
Description
Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use.
Product
Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →