RAPIDPoint® 500e Blood Gas System
Brand(s)
Last updated
Summary
Product
RAPIDPoint® 500e Blood Gas System
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 catalog number |
|---|---|---|
RAPIDPoint® 500 System - Main Unit |
All lots. |
10492730 |
RAPIDPoint® 500e Blood Gas System |
All lots. |
11416751 |
Issue
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Chemistry
Companies
Siemens Healthcare Diagnostics Inc.
511 Benedict Ave, Tarrytown, New York, United States, 10591
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74411
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