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The official notice did not include a photo. Check the product details and identifiers below.
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An official Health Canada notice concerns Rapidpoint® 500e blood gas system. Siemens Healthcare Diagnostics Inc. Has determined that two drugs, perhexiline maleate and atomoxetine hydrochloride, may interfere with sodium results that are reported on the RAPIDPoint® 500 and RAPIDPoint® 500e Blood Gas Systems. Recall start date: October 2, 2023 Published 2023-10-12.
What to do now
Contact the manufacturer if you require additional information.
Recall number
74411
Official notice
2023-10-12
The hazard
The hazard
Siemens Healthcare Diagnostics Inc. Has determined that two drugs, perhexiline maleate and atomoxetine hydrochloride, may interfere with sodium results that are reported on the RAPIDPoint® 500 and RAPIDPoint® 500e Blood Gas Systems. Recall start date: October 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
Product 2
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: Siemens, Rapidpoint® 500e Blood Gas System.
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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