Bd Angiocath Autoguard Shielded I.v. (2016-03-10)

BD ANGIOCATH AUTOGUARD SHIELDED I.V. RECALL BD Angiocath Autoguard Shielded intravenous catheters have been recalled across Canada due to a defect in the medical device. The needle guard may not function properly, which could increase the risk of needle stick injuries. The recall affects catheters distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-04
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f6bb7ef1-a35b-4547-9268-4ddcf0f42987