Medical devices• Updated Jan 3• Artis
Artis Zeego System recall in Canada: software issues
This recall involves Artis Zeego and Artis Zee medical systems sold in Canada. They are being recalled because software
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 118 of 220
Medical devices• Updated Jan 3
INTERNAL PADDLES OPTION FOR DEFIBRILLATOR/MONITOR (2020-09-17)
This recall involves INTERNAL PADDLES OPTION FOR DEFIBRILLATOR/MONITOR sold in Canada. It's being recalled because the i...
Medical devices• Updated Jan 3• CME America
CME America BodyGuard Infusion Administration Sets (2020-06-16)
This recall involves CME America BodyGuard Infusion Administration Sets sold in Canada. They are being recalled because
Medical devices• Updated Jan 3• AMS
AMS 700 MS Pump recall in Canada: device activation issues
This recall involves the AMS 700 MS (Momentary Squeeze) Pump sold in Canada. It's being recalled because of an increase
Medical devices• Updated Jan 3• Imager II
Imager II Angiographic Catheters recall in Canada: tip detachment risk
This recall involves Imager II Angiographic Catheters - 5F Curved Tip Shapes sold in Canada. They are being recalled bec...
Medical devices• Updated Jan 3• Trevo XP ProVue
Trevo XP ProVue Retriever recall in Canada: medical device may separate
This recall involves the Trevo XP ProVue Retriever medical device sold in Canada. It's being recalled because the core w...
Medical devices• Updated Jan 3
1500 Flex Heat Moisture Exchanger (2020-09-11)
This recall involves the 1500 Flex Heat Moisture Exchanger sold in Canada. It's being recalled because it may disconnect...
Medical devices• Updated Jan 3
PIPELINE FLEX EMBOLIZATION DEVICE recall in Canada: fracture risk
This recall involves the PIPELINE FLEX EMBOLIZATION DEVICE sold in Canada. It's being recalled because the device may fr...
Medical devices• Updated Jan 3• Hurricane RX
HURRICANE RX BILIARY BALLOON DILATATION CATHETER (2020-09-16)
This recall involves the Hurricane RX Biliary Balloon Dilatation Catheter sold in Canada. It's being recalled because a
Medical devices• Updated Jan 3
Uroskop Omnia & Omnia Max recall in Canada: Monitor arm may dislodge
This recall involves Uroskop Omnia and Uroskop Omnia Max urological systems sold in Canada. They are being recalled beca...
Medical devices• Updated Jan 3
Introducer Sheath recall in Canada: manufacturing defect
This recall involves certain Introducer Sheath products sold in Canada. They are being recalled due to a manufacturing d...
Medical devices• Updated Jan 3• Arthrogarde
5.5 MM Arthrogarde Hip Access Cannula recall in Canada: manufacturing error
This recall involves the 5.5 MM Arthrogarde Hip Access Cannula sold in Canada. It's being recalled due to a manufacturin...
Medical devices• Updated Jan 3
Infrared Thermometer IR 988 recall in Canada: unlicensed medical device
This recall involves the Infrared Thermometer IR 988 sold in Canada. It's being recalled because it is an unlicensed Cla...
Medical devices• Updated Jan 3• REGENEREX
REGENEREX PRIMARY TAPER recall in Canada: not properly sterilized
This recall involves REGENEREX PRIMARY TAPER medical devices sold in Canada. They are being recalled because they may no...
Medical devices• Updated Jan 3• SIGMA SPECTRUM
SIGMA SPECTRUM Infusion Pump recall in Canada: cleaning issues
This recall involves the SIGMA SPECTRUM Infusion Pump with Master Drug Library (V8 Platform) sold in Canada. It's being
Medical devices• Updated Jan 3• DEFIGARD
DEFIGARD Touch 7 recall in Canada: Device may fail to switch to AED mode
This recall involves the DEFIGARD Touch 7 medical device sold in Canada. It's being recalled because it may fail to swit...
Medical devices• Updated Jan 3
Suture-Based Repair Systems recall in Canada: packaging defect
This recall involves various Suture-Based Repair Systems from Smith & Nephew, Inc. sold in Canada. They are being recall...
Medical devices• Updated Jan 3• VICRYL
VICRYL (polyglactin 910) Suture recall in Canada: product mismatch
This recall involves one lot of VICRYL (polyglactin 910) Suture sold in Canada. It's being recalled because the product
Medical devices• Updated Jan 3
MULTIX IMPACT recall in Canada: May cause repeated radiation exposure
This recall involves the MULTIX IMPACT medical device sold in Canada. It's being recalled because unstable voltage setti...
Medical devices• Updated Jan 3• Autostainer
Autostainer Link recall in Canada: Risk of false negative results
This recall involves Autostainer Link and other Autostainer models sold in Canada. It's being recalled because an update...
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