Back to RecallTracker
Health Canada Medical devices

RAPIDPoint® 500e Blood Gas System

Issued October 12, 2023
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
Hazard description
Performance
Product
Product name
RAPIDPoint® 500e Blood Gas System
Reference
ID
RA-74411