FDASeptember 7, 2018device

V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in clinical chemistry, mon...

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

The hazard

The action is being initiated because the cooling indicator board was improperly installed. This was first noticed by a service employee during assembly. If for some reason the cooling of the reagent rotor fails, the reagent cooling indicator light will not illuminate and the acoustic beeper will not go off. As a consequence the operator will not be warned and the reagent storage conditions may fall out of specification.

What to do

FDA enforcement status: Terminated

Brands named

vital scientific n vvitalvital scientific

UPCs

14330114334415330115332618330118332303661540600180

Recall history

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

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V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, which is an automated chemistry analyzer, micro type, intended for clinical use in conjunction with certain materials to measure a variety of analytes, including applications in clinical chemistry, mon... — Recall Details · AllClear