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Dxa 5000
Official notice
30 Jun 2023
Last checked
30 Jun 2023
An official Health Canada notice concerns Dxa 5000. 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 Published 2023-06-30.
What to do now
Contact the manufacturer if you require additional information.
Recall number
73889
Official notice
2023-06-30
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Beckman Coulter Biomedical, Dxa 5000.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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