Rapidlab® 348ex System

RAPIDLab® 348EX System Recall Summary The RAPIDLab® 348EX System, a medical device used in healthcare settings, is being recalled in Canada due to a device performance issue. This recall is classified as Class II, meaning the device could potentially cause adverse health effects but is unlikely to cause serious injury or death. The recall affects units distributed across Canada.

Product
RAPIDLab® 348EX System
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-07-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/18b870ee-45a5-49dc-9261-6c1311eb3b6e