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LIASON XL Analyzer and XL System Analyzer (2015-02-02)
- Starting date:
- February 2, 2015
- Posting date:
- March 5, 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-52459
Recalled Products
A. LIAISON XL Analyzer
B. LIAISON XL System - Analyzer
Reason
A correction to parameter #61 of the Washer Dispense Pump (WDP) on the Liaison XL Analyzer is required to prevent unnecessary Washer Aspiration Failures (WAF) and Target Not Reached errors due to low dispense volume.
Affected products
A. LIAISON XL Analyzer
Lot or serial number
2210000392
2210000396
2210000786
2210000992
2210001331
Model or catalog number
I0050
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue
P.o. Box 285
Minnesota
UNITED STATES
B. LIAISON XL System - Analyzer
Lot or serial number
2210000392
2210000396
2210000786
2210000992
2210001331
Model or catalog number
I0050
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue
P.o. Box 285
Minnesota
UNITED STATES