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FDAJuly 26, 2017device

Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Potential for Intra-operative breakage of driver tips

What to do

FDA enforcement status: Terminated

Brands named

depuy orthopaedicsdepuy

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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