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Health product recall

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

  1. Liaison Xl Analyzer
  2. 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