All product recalls associated with Boston Scientific Corporation in Canada, sourced from Health Canada, Transport Canada, and the CFIA.
This recall involves the Exalt Model D Single-Use Duodenoscope sold in Canada. It's being recalled because of potential
This recall involves Emblem S-ICD Pulse Generators and Emblem MRI S-ICD Pulse Generators sold in Canada. They are being
This recall involves Guider Softip and Guider Softip Xf guide catheters sold in Canada. They are being recalled because
This recall involves Flexiva Pulse Tractip medical devices sold in Canada. They are being recalled because they were man...
This recall involves Intellanav Stablepoint Ablation Catheters sold in Canada. They are being recalled because the steri...
This recall involves the Habib™ EndoHPB Catheter, used in medical procedures. It's being recalled because of a device co...
This recall involves Orise Gel Pack and Procedure Kits sold in Canada. It's being recalled because of a performance issu...
This recall involves the Emblem MRI S-ICD PG, a medical device, sold in Canada. It's being recalled because a manufactur...
This recall involves Orise Proknife Procedure and Gel Syringe Kits sold in Canada. It's being recalled because of a perf...
This recall involves Emblem S-Icd and Latitude Programming Systems sold in Canada. They are being recalled because of a
This recall involves the Zoom Latitude Programmer/Recorder/Monitor (Prm) sold in Canada. It's being recalled because of
This recall involves Rotawire Drive Guidewire and Wireclip Torquer products sold in Canada by Boston Scientific Corporat...
This recall involves the Exalt Model D Single-Use Duodenoscope sold in Canada. It's being recalled because the instructi...
This recall involves the Spaceoar System, a medical device, sold in Canada. It is being recalled due to revised instruct...
This recall involves Hurricane RX Biliary Balloon Dilatation Catheters sold in Canada. It's being recalled because the b...