Signa™ Architect

SIGNA™ Architect Recall Summary GE Medical Systems LLC is recalling SIGNA™ Architect devices distributed across Canada due to a device performance issue. This is classified as a Class II recall, indicating a serious problem that could cause incorrect patient results or temporary health issues. The recall affects SIGNA™ Architect systems that were distributed throughout Canada.

Product

SIGNA™ Architect

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-10-16

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5e8d1531-e2a0-4fe5-85b3-a8a3b7c1c961