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XPRECIA STRIDE COAGULATION ANALYZER (2016-07-27)
- Starting date:
- July 27, 2016
- Posting date:
- August 5, 2016
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-59714
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.
Affected products
A. XPRECIA STRIDE COAGULATION ANALYZER
Lot or serial number
100889
100894
101092
101173
101787
101791
101792
Model or catalog number
10714596
Companies
- Manufacturer
-
Siemens Healthcare Diagnostics Inc.
511 Benedict Ave
Tarrytown
10591
New York
UNITED STATES