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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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5 records meeting your search criteria returned- Product Code: LQL Patient Problem: Misdiagnosis Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
BIOMERIEUX, INC. VITEK® 2 GP ID TEST KIT 10/04/2019
BIOMERIEUX, INC. VITEK® 2 GP ID TEST KIT 09/18/2018
BIOMERIEUX INC. VITEK® 2 GP TEST KIT 09/11/2017
BIOMERIEUX, INC VITEK® 2 GRAM-POSITIVE (GP) IDENTIFICATI 07/05/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 12/29/2016
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