Epiq 5 Ultrasound System (2021-08-05)

EPIQ 5 Ultrasound System Recall Summary Philips is recalling the EPIQ 5 Ultrasound System across Canada due to a medical device issue classified as Class I, which indicates a serious safety concern. The recall affects ultrasound systems distributed throughout Canada. This is a Class I recall, meaning there is a reasonable probability that use of the device could cause serious adverse health consequences or death.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-08-19

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5c5785ab-cc0b-4468-a9fa-711dfa021e6c