Epiq Diagnostic Ultrasound System

EPIQ Diagnostic Ultrasound System Recall The EPIQ Diagnostic Ultrasound System is being recalled in Canada due to a performance issue. This recall affects ultrasound systems that were distributed across Canada. The recall is classified as Class I, indicating a serious concern with how the device is functioning.

Product
EPIQ Diagnostic Ultrasound System
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-10-19
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/de2e548f-7de0-4c0f-b0ac-d19255511c0a