Medical devices• Updated Jan 3• Siemens
Siemens Dimension Software recall in Canada: potential for intermittent failures
This recall involves Siemens Dimension Software Version 10.2.2 used in various medical devices sold in Canada. It's bein...
Medical Device Recalls in Canada
Medical device recalls in Canada cover implants, surgical equipment, and diagnostic tools. These recalls are issued by Health Canada.
4,400 recalls found
Page 194 of 220
Medical devices• Updated Jan 3• CyPass
CyPass Micro-Stent recall in Canada: May cause cell loss
This recall involves the CyPass Micro-Stent Model 241, a medical device. It's being recalled because it may cause signif...
Medical devices• Updated Jan 3• THERAKOS CELLEX
Cellex Photopheresis System recall in Canada: Thromboembolic events
This recall involves the Cellex Photopheresis System used in Canada. It's being recalled because of reports of thromboem...
Medical devices• Updated Jan 3• Ovation
Ovation Abdominal Stent Graft System recall in Canada: polymer leaks
This recall involves Ovation, Ovation Prime, and Ovation IX Abdominal Stent Graft Systems used in Canada. They are being...
Medical devices• Updated Jan 3
Oxylog 3000 recall in Canada: Software defect
This recall involves the Oxylog 3000 medical device sold in Canada. It's being recalled because a software defect may pr...
Medical devices• Updated Jan 3• Polyflux Revaclear Max Dialyzer
Polyflux Revaclear Max Dialyzer recall in Canada: labeling error
This recall involves one lot of Polyflux Revaclear Max Dialyzer sold in Canada. It's being recalled because some dialyze...
Medical devices• Updated Jan 3
Hexapod Strut recall in Canada: May cause instability
This recall involves Hexapod Strut medical devices sold in Canada. They are being recalled because a manufacturing defec...
Medical devices• Updated Jan 3• Ambu
Ambu Aura40 Standard Reusable Laryngeal Mask recall in Canada: packaging error
This recall involves the Ambu Aura40 Standard Reusable Laryngeal Mask sold in Canada. It's being recalled because it may...
Medical devices• Updated Jan 3
Multi-Drug Screen Test ECO II Cup recall in Canada: Labeling error
This recall involves the Multi-Drug Screen Test ECO II Cup sold in Canada. It's being recalled because the product name
Medical devices• Updated Jan 3• Citadel Plus
Citadel Plus recall in Canada: Medical device software defect
This recall involves the Citadel Plus medical bed sold in Canada. It's being recalled because a software defect could ca...
Medical devices• Updated Jan 3• Thermablate
Consumer product recall in Canada: Thermablate devices have updated warnings
This recall involves Thermablate Disposable Cartridges and Thermablate Treatment Control Unit Kits sold in Canada. The m...
Medical devices• Updated Jan 3
DX-D 600 recall in Canada: Equipment may fall
This recall involves the DX-D 600 medical device sold in Canada. It's being recalled because parts of the equipment coul...
Medical devices• Updated Jan 3• Mammotome Revolve
Mammotome Revolve probes recall in Canada: Packaging error
This recall involves Mammotome Revolve Stereotactic Probes and Mammotome Revolve Ultrasound Probes sold in Canada. They
Medical devices• Updated Jan 3• Parapost Plus Ti5
Parapost Plus Ti5 recall in Canada: Incorrect packaging
This recall involves Parapost Plus Ti5, a medical device sold in Canada. It's being recalled because a specific batch wa...
Medical devices• Updated Jan 3• TempSure Vitalia
TempSure Vitalia recall in Canada: Claims not cleared in license
This recall involves TempSure Vitalia medical devices sold in Canada. It's being recalled because the claims made about
Medical devices• Updated Jan 3• uTASWako
uTASWako DCP and uTASWako AFP-L3 recall in Canada: incorrect label information
This recall involves uTASWako DCP and uTASWako AFP-L3 medical devices sold in Canada. They are being recalled because of...
Medical devices• Updated Jan 3• VITROS
VITROS 5600 Integrated System recall in Canada: incorrect test results
This recall involves the VITROS 5600 Integrated System used in healthcare settings in Canada. It's being recalled becaus...
Medical devices• Updated Jan 3
Thio med w/ dex, hem, vit k (10mL) recall in Canada: performance failure
This recall involves Thio med w/ dex, hem, vit k (10mL) sold in Canada. It's being recalled because it intermittently fa...
Medical devices• Updated Jan 3
Optical Surface Monitoring System (OSMS) (2018-08-10)
This recall involves the Optical Surface Monitoring System (OSMS) used with Varian TrueBeam linac systems in Canada. It'...
Medical devices• Updated Jan 3• Heartstart
Heartstart Defibrillation Pads recall in Canada: labeling confusion
This recall involves Heartstart Defibrillation Pads (M5072A) sold in Canada. They are being recalled because of incorrec...
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