Epiq Diagnostic Ultrasound System (2021-09-20)

EPIQ Diagnostic Ultrasound System Recall Philips is recalling EPIQ diagnostic ultrasound systems due to a software vulnerability that could allow unauthorized access to patient data or system functions. The recall affects EPIQ ultrasound systems distributed across Canada. This is a Class I recall, indicating a serious issue with the medical device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-10-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8703c867-a56c-4e0e-982a-f5ce263cba30