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Advia 2120 and Advia 2120I Analyzers with Autosampler (August 15, 2013)
- Starting date:
- August 15, 2013
- Posting date:
- August 15, 2013
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-35533
Reason
Siemens Healthcare Diagnostics is conducting a recall for Advia 2120/2120I Hematology systems that are connected to Avdia Autoslide systems (SMN 10286141 or SMN 10286142). Siemens has determined that if an autosampler rack jam error occurs during operation of an Advia 2120/2120I connected to an Advia Autoslide, it is possible that the next slide processed by the Autoslide could be labeled with the wrong sample identification information.
Affected products
A. Advia 2120i Analyzer with Autosampler
Lot or serial number
IR03160918, IR03480920, IR05220942, IR05230942, IR05470947, IR05480947, IR07341021, IR07361021, IR24131206, IR24141206
Model or catalog number
10361798
Companies
- Manufacturer
- Not Applicable
B. Advia 2120 System with Autosampler
Lot or serial number
IR07580542, IR07600542, IR08740603, IR09290607, IR09590610, IR20800902, IRL19450811
Model or catalog number
10316162
Companies
- Manufacturer
- Not Applicable
- Date modified: