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Rapidpoint® 500e blood gas system
Official notice
12 Oct 2023
Last checked
12 Oct 2023
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 VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Affected products
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Company & contacts
Company & contacts
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Manufacturer
Phone
Brand: Siemens, Rapidpoint® 500e Blood Gas System.
Source & status
Source & status
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Classification
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Recall details
Recall details
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Classification
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Documents, notices & source
See the official notice and source documents for full details.
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