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D-10 Haemoglobin Testing System - Analyzer (2014-03-14)
- Starting date:
- March 14, 2014
- Posting date:
- April 22, 2014
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-39159
Recalled Products
D-10 Haemoglobin Testing System - Analyzer
Reason
D-10 software version 3.60 could potentially produce duplicate results. Sample results may be duplicated and attributed to subsequent sample identifiers or injection numbers.
Affected products
D-10 Haemoglobin Testing System - Analyzer
Lot or serial number
Version 3.60
Model or catalog number
220-0220
Companies
- Manufacturer
-
Bio-Rad Laboratories Clinical Diagnostics Group
4000 Alfred Nobel Drive
Hercules
94547
California
UNITED STATES