FDAOctober 15, 2021device

Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10284473 (US) and 10488224 (OUS)

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

The hazard

Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five Dimension Vista Assays

What to do

FDA enforcement status: Terminated

Brands named

siemens healthcare diagnosticssiemenssiemens healthcare

UPCs

0063041494958100630414989556

Recall history

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

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