Dxc 500i Clinical Analyzer And Dxc 500 Au Clinical Chemistry Analyzer

Recall Summary Beckman Coulter is recalling the DxC 500i Clinical Analyzer and DxC 500 AU Clinical Chemistry Analyzer due to a device performance issue. These clinical laboratory analyzers are distributed across Canada and used in healthcare settings to process patient blood samples. The recall is classified as Class II, indicating a potential health risk situation.

Recalling firm

Beckman Coulter, Inc.

Product

DxC 500i Clinical Analyzer and DxC 500 AU Clinical Chemistry Analyzer

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-10-26

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4430ac50-5f04-4686-8099-d1f17e1a8335