DePuy Orthopaedics, Inc. recalls Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use i…
- Recall date
- July 26, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0848-2018
- FDA classification
- Class II
- Brand / firm
- DePuy Orthopaedics, Inc.
- Sold / distributed
- Nationwide Distribution
Why it was recalled
Potential for Intra-operative breakage of driver tips
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
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