Health Canada — Medical Devices · Canada · 2017-03-15 · Type II
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Reported risk: Following a production change of connector types for the sample probe plug, it was confirmed by the manufacturer that in very rare cases, a disturbance of the sample liquid level detection (LLD) may occur. This may cause the affected sample probe to dip into the sample material deeper than intended, causing the affected sample probe to be washed inadequately and lead to a potential carryover.
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