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Smith & Nephew, Inc. recalls smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)
Recalled June 20, 2018 · FDA recall Z-2163-2018 · Smith & Nephew
Hazard
One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification. · FDA Class II
Units
5 units
Sold at
International only: United Arab Emirates, Spain, Mexico
Description
One lot of GENESIS II 13 mm tibial punches are 2 mm smaller than specification.
Product
smith&nephew GENESIS(R) II TIBIAL Punch, 13 MM, REF 71440408, QTY: (1)
Manufacturer(s)
Smith & Nephew, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →