Product Wiki · Recalls · Health Canada — Medical Devices

ARCHITECT C8000 Analyzer, ARCHITECT C16000/C4000 Processing Module… — recall 57930

Health Canada — Medical Devices · Canada · 2017-12-21 · Type II

As described by Health Canada — Medical Devices: ARCHITECT C8000 Analyzer, ARCHITECT C16000/C4000 Processing Module and ARCHITECT C4000 Integrated Processing Module (2017-12-13)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
57930
Date of alert
2017-12-21
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: The base of the ARCHITECT Cuvette Segment may become detached under specific conditions. When a cuvette segment base is detached, cuvettes may be seated lower than the designed height. This may result in inadequate dispense into specific cuvettes due to the sample probe being unable to make efficient contact with the cuvette bottom.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/architect-c8000-analyzer-archi

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