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LIAISON SYSTEM - RUBELLA IGG ASSAY (2015-01-28)
- Starting date:
- January 28, 2015
- Posting date:
- July 7, 2015
- 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-54088
Recalled Product
A.LIAISON SYSTEM - RUBELLA IGG ASSAY
Reason
Potential for increased frequency of invalid calibrations of the LIAISON Rubella IgG assay due to low calibrator deviations.
Affected products
A.LIAISON SYSTEM - RUBELLA IGG ASSAY
Lot or serial number
- 019030X
- 019030X/1
Model or catalog number
310460
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue
P.o. Box 285
Minnesota
UNITED STATES