Product Wiki · Recalls · Health Canada — Medical Devices

Siemens Dimension Vista (2016-03-30) — recall 55062

Health Canada — Medical Devices · Canada · 2016-04-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
55062
Date of alert
2016-04-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Siemens Healthcare Diagnostics has received customer complaints of discrepant patient results on Dimension Vista Intelligent Lab Systems. Siemens Healthcare Diagnostics has confirmed a software defect which, in a very specific set of circumstances, results in the Dimension Vista System omitting an aliquot probe rinse between sample aspirations when processing tubes in sample racks that are front loaded on the Dimension Vista System. Omission of the aliquot probe rinse may result in carryover of residual sample estimated up to 10% when the sample is dispensed into the aliquot well. Carryover of residual sample from the outside of the aliquot probe into the sample tube is estimated at less than 0.1%.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/siemens-dimension-vista-2016-0

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