FDASeptember 12, 2017device

i-STAT DE handheld data processing module for clinical use, Software Version 2.8, List Number:08K46-01115200 (UDI: 00054749001255)

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

The hazard

Issues resulting from upgrade to software version 2.8: (1) Location, operator, stored patient lists will not update, and (2) Customized Reference Ranges, Action Ranges, and Custom Reportable Ranges are reset to factory default values. No erroneous results are generated as a result of this issue.

What to do

FDA enforcement status: Terminated

Brands named

abbott pointabbott

UPCs

00054749001255

Recall history

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

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