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FDAFDA · Alimentos y medicamentos·N.º oficial Z-0949-2014

The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The instrument can perform screening for abnormal samples with a high degree of accuracy, so it increases automation and efficiency in laboratories.

Publicado el 19 de febrero de 2014 · Inicio del retiro: 31 de marzo de 2013

Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.

Qué peligro representa

The current Century Break patch did not contain the same setting for the Century Break year for both the Red Hat Linux and GUI files. Due to the mismatch in file settings, the software could not properly calculate a purge date for the database files based on the customer data retention setting in the application. This resulted in the database files meeting its maximum capacity and causing system p

Qué hacer

Voluntary: Firm initiated · Letter

Detalles del retiro

Fabricante
Sysmex America, Inc.
Distribuidor
Worldwide Distribution - USA (nationwide) Distribution including Puerto Rico and the states of AL, AR, CA, CO, CT, FL, GA, HI, IA, IS, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA and WI and the country of Canada.
Lote
Software versions 1.0, 1.01, 1.1.1, 1.1.2
Clasificación de riesgo
Class II
Área (FDA)
device
País
United States

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