Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 40 of 220
This recall involves Advanta and Flixene Vascular Grafts sold in Canada. They are being recalled because of a potential
This recall involves Philips Ingenia medical devices sold in Canada. It's being recalled because oil may leak, creating
This recall involves InstaClear Sheath medical devices sold in Canada. It's being recalled because the sheath's plate or...
This recall involves BD SARS-CoV-2 Reagents for the BD Max System sold in Canada. It's being recalled because the assays...
This recall involves Stardrive Screwdriver Shafts sold in Canada. They are being recalled because they were manufactured...
This recall involves the ComboLab System sold in Canada. It's being recalled because a component could fail, affecting t...
This recall involves the Philips Hemodynamic Application software used in medical devices in Canada. It's being recalled...
This recall involves BD Synapsys Version 4.10, a medical device, sold in Canada. It's being recalled because of two soft...
This recall involves Synchro Guidewires sold in Canada. They are being recalled because of potential performance issues
This recall involves PAED Pack medical devices sold in Canada. They are being recalled because of potential performance
This recall involves Omnilab Advanced Domestic and Omnilab Advanced Domestic Core devices sold in Canada. They are being...
This recall involves Luer Slip and Luer Lock Syringes from Medline Industries, LP sold in Canada. They are being recalle...
This recall involves the MED-RX® Epidural Anesthesia Kit sold in Canada. It's being recalled because the depth markers o...
This recall involves the HistoCore Arcadia H, a medical device, sold in Canada. It's being recalled because a defect cou...
This recall involves Stryker ProCuity Beds sold in Canada. They are being recalled because manufacturing records are mis...
This recall involves the Integra Cranial Kit sold in Canada. It's being recalled because the sterile packaging may have
This recall involves MyoSPECT Molecular Imaging devices sold in Canada. It's being recalled because the lead cover servi...
This recall involves Presource® Kits containing Curity® Flexible Adhesive Bandage X-large Components sold in Canada. The...
This recall involves Ultra Intra-Aortic Balloon Pumps (IABP) sold in Canada. They are being recalled because of a perfor...
This recall involves Medline Control Syringe Fixed Male Luer Lock sold in Canada. It's being recalled because of potenti...
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