Cadd-solis Ambulatory Infusion Pump

Recall Summary The CADD-Solis Ambulatory Infusion Pump is being recalled in Canada due to a performance issue. This pump is a medical device used to deliver medications to patients. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device's performance.

Product
CADD-Solis Ambulatory Infusion Pump
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-04-23
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1ac0c012-061d-4642-969a-b95725b3a099