FDAFebruary 5, 2019device

Intersomatic JULIET Ti OL cage. For use in orthopedic spinal procedures

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

The hazard

Inner blister pack label is incorrect and does not match the correct external box label.

What to do

FDA enforcement status: Terminated

Brands named

spineart saspineart

UPCs

07640178973985

Recall history

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

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