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FDADecember 16, 2015device

AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device system that uses hydraulic pressure to expand the implant in-situ. The purpose of the AccuLIF PL Tubing Set (cat#900301) and AccuLIF TL Tubing Set (cat#905103) is to deliver pressurized saline from a syringe to the Acc...

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

The hazard

There were two potential interference conditions identified with the way the tubing set attaches to the inserter.

What to do

FDA enforcement status: Terminated

Brands named

stryker spinestryker

Recall history

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

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AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF is an interbody device system that uses hydraulic pressure to expand the implant in-situ. The purpose of the AccuLIF PL Tubing Set (cat#900301) and AccuLIF TL Tubing Set (cat#905103) is to deliver pressurized saline from a syringe to the Acc... — Recall Details · AllClear