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Liaison XI Analyzer and System Analyzer (2017-07-01)
- Starting date:
- July 1, 2017
- Posting date:
- August 14, 2017
- 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-64112
Affected Products
- Liaison Xl Analyzer
- Liaison Xl System - Analyzer
Reason
The affected Liaison XL label "I" barcode labels may cause an instrument error when being read by the barcode scanner making the rack unusable. Control results can be obtained by changing the position of the control in the rack or manual entry of the control information. It is unlikely that patient results would be adversely affected by the Liaison XL label "I" barcode labels.
Affected products
A. Liaison Xl Analyzer
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
I0050
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue, P.O. Box 285
Stillwater
55082
Minnesota
UNITED STATES
B. Liaison Xl System - Analyzer
Lot or serial number
More than 10 numbers, contact manufacturer
Model or catalog number
I0050
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue, P.O. Box 285
Stillwater
55082
Minnesota
UNITED STATES