Product Wiki · Recalls · Health Canada — Medical Devices

epoc Blood Analysis BGEM Test Card — recall 77251

Health Canada — Medical Devices · Canada · 2025-04-09 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
77251
Date of alert
2025-04-09
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Chemistry
Product type
Medical devices
Reported risk: Siemens confirmed that the occurrence of discrepant high pH results in samples introduced with higher injection volumes (beyond the epoc reader beep or after the "analyzing sample" message is displayed) with epoc sensor configuration 45.n (software version: epoc host v3.41.2 and epoc nxs v4.14.9 & 4.14.11) Recall start date: March 25, 2025
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/epoc-blood-analysis-bgem-test-

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