Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 44 of 220
This recall involves the MIS Sterile Instrument Pack sold in Canada. It's being recalled because the beaver blade handle...
This recall involves Applied Medical Clip Appliers sold in Canada. It's being recalled because the device may not load c...
This recall involves Auto Suture Blunt Tip and Structural Balloon Trocars sold in Canada. They are being recalled due to...
This recall involves the Trident II Clusterhole HA Acetabular Shell sold in Canada. It's being recalled because of a pot...
This recall involves various Olympus Medical Endoscopes sold in Canada. They are being recalled due to issues with label...
This recall involves Cardinal Health Cardiovascular, Bypass, and Hepatobiliary Packs sold in Canada. They are being reca...
This recall involves the Agfa Digital Radiography Mobile X-Ray System Dx-D 100 sold in Canada. It's being recalled becau...
This recall involves Impella medical devices sold in Canada. New warnings are being added to the instructions for use to...
This recall involves Baxter Flo-Thru, Flo-Rester, and Vascular Probe medical devices sold in Canada. They are being reca...
This recall involves Raystation medical devices sold in Canada. It's being recalled because of a performance issue relat...
This recall involves the Thermalon Sinus Mask sold in Canada. It's being recalled because it may have mold or mildew due...
This recall involves Parapac Plus 310 Ventilators sold in Canada. They are being recalled because they may not cycle pro...
This recall involves Vitros® Systems medical devices sold in Canada. They are being recalled because a hardware part may...
This recall involves Origio Sperm Wash sold in Canada. It's being recalled because it has an insufficient concentration
This recall involves several Medline irrigation and flush products sold in Canada. They are being recalled because of a
This recall involves the Vantage Orian MRI system. It's being recalled because a terminal block issue can cause arcing a...
This recall involves Heartmate II and Heartmate 3 Left Ventricular Assist Systems sold in Canada. They are being recalle...
This recall involves Impella Systems sold in Canada. It's being recalled because updated instructions for use include ne...
This recall involves the BD Bodyguard Microset, a medical device sold in Canada. It's being recalled because the clamp o...
This recall involves Erich Arch Bar Roll and Obwegeser Raspatory medical devices sold in Canada. They are being recalled...
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