LIAISON XL System Analyzer (2019-05-07)
- Starting date:
- May 7, 2019
- Posting date:
- June 7, 2019
- 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-70109
Last updated: 2019-06-07
Affected Products
- LIAISON XL Analyzer
- LIAISON XL System Analyzer
Reason
Internal investigation has confirmed there is a potential for breakage of the POM Stirrer Bar, P/N 100001612. The POM Stirrer Bar was pre-installed onto the LIAISON XL Analyzer. In order to avoid this issue, the POM Stirrer Bar has been redesigned.
Affected products
A. LIAISON XL Analyzer
Lot or serial number
2210003580
2210003635
2210003738
2210003745
2210003853
2210004149
2210004199
2210004267
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
2210003580
2210003635
2210003738
2210003745
2210003853
2210004149
2210004199
2210004267
Model or catalog number
I0050
Companies
- Manufacturer
-
Diasorin Inc.
1951 Northwestern Avenue, P.O. Box 285
Stillwater
55082
Minnesota
UNITED STATES