Absolute Pro Ll .035 Peripheral Self-Expanding Stent System
This recall involves the Absolute Pro Ll .035 Peripheral Self-Expanding Stent System. It's being recalled because of pot...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 81 of 220
This recall involves the Absolute Pro Ll .035 Peripheral Self-Expanding Stent System. It's being recalled because of pot...
This recall involves Bond Wash Solution sold in Canada. It's being recalled because of a device compatibility issue that...
This recall involves Surestrips Covid-19 Antigen Tests sold in Canada. They are being recalled because they are not auth...
This recall involves Philips Medical Systems Pagewriter TC70 and TC50 Electrocardiographs sold in Canada. They are being...
This recall involves Ortho Connect medical devices sold in Canada. It's being recalled because of a software defect. Sto...
This recall involves Poches A Sang Quadruple, a medical device used in healthcare settings. It's being recalled because
This recall involves the ABL800 Flex System, a medical device used in healthcare settings. It's being recalled because o...
This recall involves Ks White Nitrile Medical Examination Gloves sold in Canada. They are being recalled because they do...
This recall involves Alinity Hs/Hq System medical devices sold in Canada. It's being recalled because of a performance i...
This recall involves the Carescape Central Station sold in Canada. It's being recalled because of a potential electrical...
This recall involves the Argyle Safety Fistula Cannula with Anti-Reflux Valve sold in Canada. It's being recalled becaus...
This recall involves the SoClean 2 Automated Supplemental PAP Maintenance Device sold in Canada. It's being recalled bec...
This recall involves Belotero Lidocaine products sold in Canada. It's being recalled because temperature changes during
This recall involves plasma pens sold in Canada. They are being recalled because they are unauthorized medical devices a...
This recall involves unauthorized plasma pens sold in Canada. They are being recalled because they have not been evaluat...
This recall involves the Citadel Bed Frame System sold in Canada. It's being recalled because a metal part of the device...
This recall involves the Bililux medical device sold in Canada. It's being recalled because a manufacturing defect could...
This recall involves Primus Anaesthetic Workstations sold in Canada. They are being recalled because of a manufacturing
This recall involves Nim™ Standard Reinforced Emg Endotracheal Tube and Nim Contact™ Reinforced Emg Endotracheal Tube so...
This recall involves the Breathing System Filter Safestar 55 sold in Canada. It's being recalled because an obstructed f...
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