Perimeter Octopus 900 recall in Canada: Medical device data error
This recall involves the Perimeter Octopus 900 medical device sold in Canada. It's being recalled because it may lose da...
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 163 of 220
This recall involves the Perimeter Octopus 900 medical device sold in Canada. It's being recalled because it may lose da...
This recall involves 3T Heater-Cooler Devices sold in Canada. It's being recalled because of a design upgrade to the vac...
This recall involves Tina-Quant IgA Gen2 (IgA-2) medical devices sold in Canada. It's being recalled because of potentia...
This recall involves Artis Zeego Multi-Axis, Zee Floor, Zee Ceiling, Zee Biplane, and Artis Q medical devices sold in Ca...
This recall involves Revolution CT - Main Unit and Revolution CT ES medical devices sold in Canada. They are being recal...
This recall involves Alinity i BNP Calibrators sold in Canada. They are being recalled because they may give falsely ele...
This recall involves the Stratus CS Acute Care System Cardiac troponin-i TestPak sold in Canada. It's being recalled bec...
This recall involves MAGNETOM Vida and Sola medical devices sold in Canada. They are being recalled because of software
This recall involves the MicroEtcher CD KaVo handheld dental sandblasting unit sold in Canada. It's being recalled becau...
This recall involves M.I.C.E. Penicillin 32, a medical device used for testing. It's being recalled because it produces
This recall involves Filter-Tips, 1500 μl (1024) sold in Canada. They are being recalled because a small percentage of t...
This recall involves Assayed Bovine Multi-Sera - Level 1 sold in Canada. It's being recalled because the target and rang...
This recall involves all lots of the Tritanium PL Cage, a medical device, sold in Canada. It's being recalled because it...
This recall involves REVACLEAR Dialyzers distributed in Canada. They are being recalled because ruptured fibers could le...
This recall involves the ZOLL AED Pro External Defibrillator sold in Canada. It's being recalled because it may fail to
This recall involves the Sensis medical device sold in Canada. It's being recalled because a software update provides ma...
This recall involves the Salivary Testosterone ELISA medical device sold in Canada. It's being recalled because it may g...
This recall involves various Medline custom procedure packs sold in Canada. They are being recalled because the anti-fog...
This recall involves the SLIM Handle medical device sold in Canada. It's being recalled because a connector ring inside
This recall involves Premier Soft Convex CeraPlus Tape Bordered Barrier products sold in Canada. It's being recalled bec...
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