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VGI Medical, LLC recalls VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit
Recalled June 13, 2018 · FDA recall Z-2100-2018 · VGI Medical
Hazard
IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated · FDA Class II
Units
6 units
Sold at
Distributed to MI, FL, and NY.
Description
IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated
Product
VGI MEDICAL VerteLP LATERAL INTERBODY FUSION instrument kit
Manufacturer(s)
VGI Medical, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →