FDAJune 24, 2025device

PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-3713SP

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

The hazard

A 37 mm implant width intervertebral body fusion device has a labeling discrepancy with incorrect width of 33 mm stated on the outer label side flap and inner label side flap information box. The 37 mm width on the front labels is correct.

What to do

FDA enforcement status: Ongoing

Brands named

orthofix u sorthofix

UPCs

18257200161010

Recall history

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

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