Dxa 5000
Brand(s)
Last updated
Summary
Product
Dxa 5000
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
Dxa 5000 |
Not applicable. |
B50516 |
Issue
The dxa software has configuration settings to identify tests that are not to be performed based upon a specific tube type. The dxa does not communicate this to the remisol middleware software quickly enough to prevent the test to be run.
Recall start date: June 2, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Pathology
Companies
| Beckman Coulter Biomedical Gmbh |
| Sauerbruchstr 50, Muenchen, Germany, 81377 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73889
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