Home / Recalls / Medical Devices
Luminex Corporation recalls Verigene EP Amplification Reagent Kit Test
Recalled September 22, 2021 · FDA recall Z-2451-2021 · Luminex
Hazard
There is potential for false positive results. · FDA Class II
Units
4579 kits
Sold at
Worldwide distribution - US Nationwide distribution and the countries of Austria, France, Greece, Japan, and Turkey.
Description
There is potential for false positive results.
Product
Verigene EP Amplification Reagent Kit Test
Manufacturer(s)
Luminex Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →