Dxc 500i Clinical Analyzers

DxC 500i Clinical Analyzers Recall DxC 500i Clinical Analyzers are being recalled in Canada due to performance issues. This Class I recall affects the devices distributed across Canada. These are laboratory instruments used in clinical settings to analyze patient samples.

Product
DxC 500i Clinical Analyzers
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-08-19
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a19ad8cb-a4f0-4cea-bb9b-f4290735c680