Rrow 3-lumen, 8.5 Fr Cvc Kits (2018-05-11)

Recall Summary ARROW 3-Lumen, 8.5 Fr CVC Kits are being recalled across Canada due to a defect in the medical device. These kits are central venous catheters used in medical settings for intravenous access. The recall is classified as Class I, which is the most serious category.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-06-01

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/524a3a35-d462-4376-9b99-a74a443f59cb