Nephrocare Bedside

Nephrocare Bedside Recall Summary Nephrocare Bedside is being recalled across Canada because it does not meet the required sterility standards for a product meant for internal medical use. The recall is classified as Class I, meaning there is a potential serious health risk. This recall affects all Nephrocare Bedside products distributed in Canada.

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-02-28
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cf5beae1-6a3a-45f4-a72b-b43156099a6f