FDAFebruary 12, 2021device

Precice Bone Transport - Product Usage: intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.

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

The hazard

Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

What to do

FDA enforcement status: Ongoing

Brands named

nuvasive specialized orthopedicsnuvasivenuvasive specialized

UPCs

887517981370887517981554887517981547887517981530887517981523887517981516887517981509887517981493887517981486887517981479887517981462887517981455

Recall history

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

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