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DePuy Orthopaedics, Inc. recalls Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use
Recalled March 14, 2018 · FDA recall Z-0848-2018 · DePuy Orthopaedics
Hazard
Potential for Intra-operative breakage of driver tips · FDA Class II
Units
130 units total
Sold at
Nationwide Distribution
Description
Potential for Intra-operative breakage of driver tips
Product
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Manufacturer(s)
DePuy Orthopaedics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →