MAGNETOM MRI Systems recall in Canada: pressure build-up risk
This recall involves MAGNETOM MRI Systems (Prisma, Vida, Skyra, Verio, Lumina, Cima.X) and Biograph mMR System sold in C...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 6 of 220
This recall involves MAGNETOM MRI Systems (Prisma, Vida, Skyra, Verio, Lumina, Cima.X) and Biograph mMR System sold in C...
This recall involves Philips IntelliVue Patient Monitors sold in Canada. They are being recalled because a feature that
This recall involves the OER-PRO Endoscope Reprocessor sold in Canada. It's being recalled because of a performance issu...
This recall involves the BD BACTEC™ MGIT™ 960 PZA Kit sold in Canada. It's being recalled because of issues with its lab...
This recall involves the Inlay Optima™ Ureteral Stent Without Guidewire Kit, Length 30cm, 6Fr. It's being recalled becau...
This recall involves the Tamper Evident Additive Port Cap sold in Canada. It's being recalled because the corrugated shi...
This recall involves Henry Schein Maxima Diamonds FG (Burs) sold in Canada. It's being recalled because of updated instr...
This recall involves SLSolution™ medical devices sold in Canada. They are being recalled because the reagent may lose it...
This recall involves RADspeed Pro X-Ray and CH-200, CH-200M Ceiling Tube Supports sold in Canada. They are being recalle...
This recall involves Quantum Intersegmental Tables sold in Canada. It's being recalled because the heat function can ove...
This recall involves the Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette sold in Canada. It's be...
This recall involves Access 2 Reaction Vessels sold in Canada. They are being recalled because of performance issues, in...
This recall involves the Vantage Galan 3T medical device sold in Canada. It's being recalled because a refrigerant gas l...
This recall involves ErgoStar CM 45 and ErgoStar CM 55 medical devices sold in Canada. They are being recalled because t...
This recall involves the Single Use Ligating Device PolyLoop™ sold in Canada. It's being recalled because the ligation l...
This recall involves the Aurora EV-ICD™ MRI SureScan™, a medical device. It's being recalled because a rare sequence of
This recall involves CareLink™ Software (MMT-7350) used in Canada. It's being recalled because it may display incorrect
This recall involves VACUETTE® 2 mL 9NC Coagulation Sodium Citrate 3.2% medical devices. They are being recalled because...
This recall involves Rocket Seldinger Chest Drain Kits sold in Canada. It's being recalled because of incorrect labellin...
This recall involves Olympus Medical Single Use Electrosurgical Snares sold in Canada. They are being recalled because s...
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