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Recall Observatory FDA recall evidence

Device product

Dimension Vista 500, model no. 10284473 an 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 fluids.

Z-0616-2019

October 16, 2018

Class II

Product summary

Firm
Siemens Healthcare Diagnostics, Inc.
Event
Event 81478
Status
Terminated
Classification
Class II
Quantity
1649
Official record key
device-enforcement:Z-0616-2019

Official wording

Reason: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista software v.3.7 and v.3.8.1 that may result in aliquot well contamination. If a test is cancelled by the operator while the instrument is aliquotting the sample, the Dimension Vista instrument may continue to deliver the cancelled sample or vial contents to the aliquot well(s). Future samples may be assigned to the same aliquot well(s) and become contaminated with the existing contents or overflow of the aliquot well may occur potentially contaminating a surrounding well(s). This issue only occurs when an operator manually cancels a test(s) for calibration, quality control (QC) or patient sample while the instrument is in the process of aliquotting the sample.

Code information: Dimension Vista software versions 3.7 and 3.8.1

Distribution pattern: Nationwide/worldwide distribution.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    issue with Dimension Vista software