Res Catheter (2020-12-08)

ARES Catheter Recall Summary The ARES Catheter has been recalled across Canada due to a medical device issue. This recall is classified as Class I, indicating a serious safety concern. The product was distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-12-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ecc64f56-1f74-4b01-92a1-515b132ef016