Carestation 850

Carestation 850 Recall Summary Carestation 850 patient monitoring devices are being recalled in Canada due to a device performance issue. The recall is classified as Class II, meaning the device could cause temporary or reversible health effects. The devices were distributed across Canada.

Product
Carestation 850
Reason
Device performance issue
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-08-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/746d1776-1cee-4d6c-99f3-6c12467e1082