Health product recall

DxC 500 AU Clinical Chemistry Analyzer

Last updated

Summary

Product
DxC 500 AU Clinical Chemistry Analyzer
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

DxC 500 AU Clinical Chemistry Analyzer

2024070118

C63520
C63519

Issue

Beckman Coulter has determined that the DxC 500 AU Clinical Chemistry Analyzer might assign a test result to an incorrect sample ID under the following workflow conditions. After loading a barcoded sample tube (sample A) onto the DxC 500 AU Clinical Chemistry Analyzer, all tests ordered for that barcoded sample tube are locked into the specific position of that barcoded tube on the analyzer (for example, the position on the DxLab rack or position in the stat table) until all tests are completed or cancelled for that sample tube. A problem might occur if, for any reason, all tests ordered for that barcoded sample tube (sample A) are not completed or remain "in pending", and the operator attempts to analyze a second sample tube (sample B) in that same position on the rack or stat table. If the bar code for sample B is not successfully scanned by the analyzer or if the sample tube is not labelled, the analyzer assumes the sample that previously occupied that position has been reloaded (sample A). The analyzer will complete and report the pending tests associated with sample A, using sample B. No results will be reported for sample A. This issue does not arise if all barcoded sample tubes are successfully scanned or if testing is complete for the first barcoded sample (sample A). 

Recall Start Date: March 7, 2025

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Chemistry
Companies

Beckman Coulter, Inc.

250 S. Kraemer Blvd., Brea, California, United States, 92821

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77175

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