FDAApril 9, 2018device

VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit

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

The hazard

IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated

What to do

FDA enforcement status: Terminated

Brands named

vgi medicalvgi

UPCs

162402163203

Recall history

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

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