OFFICIAL-SOURCE RECALL · CANADA
Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Recall: Beckman Coulter identified a software
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Analyzer
- Manufacturer
- See official notice
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples. Following user configuration of a chemistry test to nondefault units, subsequent activation of a draft configuration in the system configuration page may revert units to the system default without notifying the user.
Hazard
Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples. Following user configuration of a chemistry test to nondefault units, subsequent activation of a draft configuration in the system configuration page may revert units to the system default without notifying the user.
Official recall notice
Dxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Analyzer
Agency: Health Canada
Official publication date: September 10, 2026
Read the official CANADA_HEALTH recall notice →SCAN ONCE. KEEP WATCHING.
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