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20/12/16
21:08
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I missed this one until recently
http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/59714r-eng.php
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Affected products
A. XPRECIA STRIDE COAGULATION ANALYZER
Reason
Siemens has confirmed that version (v1.0) of the data management software (DMS) CD was packaged with some Xprecia Stride Coagulation Analyzers. The version of the DMS CD should have been v1.1, as this will match the version of firmware pre-loaded on the analyzer. These two versions must match in order to provide full functionality to the analyzer.
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Stride recall due to software version error in the analyser. Sounds like an easily rectified issue
Ill take this as positive news that the Stride system is actually being sold and getting out there into the market.
Last edited by
Gappa :
20/12/16