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Stryker Howmedica Osteonics Corp. recalls Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
Recalled January 23, 2013 · FDA recall Z-0695-2013 · Stryker Howmedica Osteonics
Hazard
Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients. · FDA Class II
Units
476 units
Sold at
Nationwide Distribution, including the states of PA, OH, NY, CA and IL.
Description
Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients.
Product
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →