Medical devices• Updated Jan 3
Naida Cl Q70 sound processor recall in Canada: Mislabeled device name
This recall involves the Naida Cl Q70 sound processor sold in Canada. It's being recalled because the device name is mis...
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 178 of 220
Medical devices• Updated Jan 3• MED-RX
MED-RX Feeding Tube recall in Canada: Incorrect product in package
This recall involves MED-RX Feeding Tubes sold in Canada. It's being recalled because the package contains an incorrect
Medical devices• Updated Jan 3• Medtronic
Medtronic Stent Graft Systems recall in Canada: sterile barrier compromised
This recall involves Medtronic Stent Graft Systems sold in Canada. They are being recalled because the sterile barrier m...
Medical devices• Updated Jan 3
Fistula Wound Crown, Fistula Funnel, Isolator Strip (2019-01-25)
This recall involves the Fistula Wound Crown, Fistula Funnel, and Isolator Strip sold in Canada. It's being recalled bec...
Medical devices• Updated Jan 3• Acuson
Acuson NX3 recall in Canada: Risk of burns or tissue damage
This recall involves Acuson NX3 and Acuson NX3 Elite ultrasound systems sold in Canada. They are being recalled because
Medical devices• Updated Jan 3• Voyager
Voyager Duo Lift recall in Canada: Interruption in motion
This recall involves the Voyager Duo Lift sold in Canada. It's being recalled because a fuse on the circuit board may bl...
Medical devices• Updated Jan 3• AXIUS
Blower/Mister recall in Canada: May cause procedural delay
This recall involves the AXIUS Blower Mister medical device sold in Canada. It's being recalled because it may fail to e...
Medical devices• Updated Jan 3
Transseptal Needle Sets recall in Canada: damage to introducer
This recall involves Transseptal Needle Sets sold in Canada. They are being recalled because they were manufactured with...
Medical devices• Updated Jan 3• UniMatch Plus
UniMatch Plus Software recall in Canada: may cause incorrect medical results
This recall involves UniMatch Plus Software used in Canada. It's being recalled because incorrect information in the sof...
Medical devices• Updated Jan 3• Herbst
Herbst Bite Jumper recall in Canada: incorrect size
This recall involves the Herbst Bite Jumper, a medical device, sold in Canada. It's being recalled because some packages...
Medical devices• Updated Jan 3• Combi
Combi Loop Sling recall in Canada: fall risk
This recall involves Combi Loop Slings sold in Canada. It's being recalled because the orange loop stitching may malfunc...
Medical devices• Updated Jan 3
PushValve and MagValve recall in Canada: increased risk for patients
This recall involves PushValve and MagValve medical devices sold in Canada. They are being recalled because a valve-inse...
Medical devices• Updated Jan 3• UniCel DxC
UniCel DxC medical devices recall in Canada: calibration failure
This recall involves UniCel DxC 600, 600i, 800, 800i, 860i, and 880i medical devices sold in Canada. It's being recalled...
Medical devices• Updated Jan 3• Feather-Flex
Feather-Flex Dual Swivel Endotracheal Adapter recall in Canada: potential leak
This recall involves the Feather-Flex Dual Swivel Endotracheal Adapter with Suction Port and Tapered Flex sold in Canada...
Medical devices• Updated Jan 3• Femilift/Pixel CO2 Laser System
Femilift/Pixel CO2 Laser System recall in Canada: Not approved for use
This recall involves the Femilift/Pixel CO2 Laser System with Femilift Handpiece sold in Canada. It's being recalled bec...
Medical devices• Updated Jan 3• VITEK 2
VITEK 2 Test Cards recall in Canada: compromised seal
This recall involves VITEK 2 Test Cards sold in Canada. They are being recalled because the top seal of the card pouches...
Medical devices• Updated Jan 3
Therapy Chair Coil Arm recall in Canada: arm may fail during use
This recall involves Therapy Chair Coil Arms sold in Canada. It's being recalled because the coil arm may fail during us...
Medical devices• Updated Jan 3
Health Canada updates breast implant safety review: BIA-ALCL risk
Health Canada is updating its safety review of breast implants in Canada. This is due to an increase in reported cases o...
Medical devices• Updated Jan 3• LIFEPAK
LIFEPAK 15 Monitor/Defibrillator recall in Canada: therapy delay risk
This recall involves LIFEPAK 15 Monitor/Defibrillators sold in Canada. They are being recalled because they may lock up
Medical devices• Updated Jan 3
T2 Femur Instrument Tray recall in Canada: Incorrect identification
This recall involves the T2 Femur Instrument Tray sold in Canada. It's being recalled because the faceplates may incorre...
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