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Smith & Nephew Inc recalls GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product Usage: orthopaedic
Recalled November 13, 2013 · FDA recall Z-0131-2014 · Smith & Nephew
Hazard
Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6 R and vice versa. · FDA Class II
Units
4 units
Sold at
USA Nationwide Distribution in the states of: AZ, NC, IA, PA, OH, MD, and TN.
Description
Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6 R and vice versa.
Product
GENESIS(R) II, NON-POROUS TIBIAL BASE, SIZE 6, RIGHT, QTY: (1), REF 71420188. Product Usage: orthopaedic
Manufacturer(s)
Smith & Nephew Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →