8f Xcela Plus Implantable Ports & 8f Bioflo Plus Implantable Ports (2019-09-18)

Recall Summary 8F Xcela Plus and 8F Bioflo Plus implantable ports are being recalled across Canada due to a defect in the medical devices. These ports are surgically implanted devices used to deliver medication or fluids. The recall is classified as Class I, which is the most serious type of recall.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-10
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3ade2371-d810-442e-89e7-e0075b2974e5