FDAJanuary 27, 2022device

LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped individually, as tray replen...

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

The hazard

Potential for weld separation of the Upper Tulip Head component from the Lower Tulip Head component, which would result in the separation of the Tulip Head from the Screw Shank.

What to do

FDA enforcement status: Terminated

Brands named

integrity implantsintegrity

UPCs

008186130277160081861302788400818613027723008186130277300081861302774700818613027754008186130277920081861302780800818613027815008186130278220081861302783900818613027846

Recall history

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

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