Medical devices• Updated Jan 3• HARMONIC
HARMONIC HD 1000I SHEARS recall in Canada: continuous activation risk
This recall involves HARMONIC HD 1000I SHEARS sold in Canada. They are being recalled because an internal component may
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 99 of 220
Medical devices• Updated Jan 3
DXA 5000 recall in Canada: Medical device defect
This recall involves the DXA 5000 medical device used in Canada. It's being recalled because sample carriers may drop of...
Medical devices• Updated Jan 3
Medical device recall in Canada: TEMPORARY CYLINDER, MULTI-UNIT
This recall involves TEMPORARY CYLINDER, MULTI-UNIT medical devices sold in Canada. They are being recalled because they...
Medical devices• Updated Jan 3• REMISOl ADVANCE
REMISOl ADVANCE recall in Canada: Medical device issue
This recall involves REMISOL ADVANCE medical devices sold in Canada. It's being recalled because a software issue could
Medical devices• Updated Jan 3• Solero
Solero Generator recall in Canada: Software error could delay medical procedures
This recall involves specific Solero Generators used in medical procedures in Canada. It's being recalled because a soft...
Medical devices• Updated Jan 3• ENDOCUFF VISION
ENDOCUFF VISION recall in Canada: Infection risk
This recall involves ENDOCUFF VISION medical devices sold in Canada. They are being recalled because a packaging defect
Medical devices• Updated Jan 3
Adult Anesthesia Breathing Circuit recall in Canada: Leaks and holes
This recall involves the Adult Anesthesia Breathing Circuit sold in Canada. It's being recalled because the tubing may h...
Medical devices• Updated Jan 3
Ultrasound Integration Software recall in Canada: incorrect depth display
This recall involves Ultrasound Integration Software for Cranial/ENT Navigation 3.1.x sold in Canada. It's being recalle...
Medical devices• Updated Jan 3• Pipeline Flex
Pipeline Flex Embolization Device recall in Canada: serious injury risk
This recall involves the Pipeline Flex Embolization Device and Pipeline Flex Embolization Device with Shield Technology
Medical devices• Updated Jan 3• Glidescope
Glidescope Go recall in Canada: May fail to meet water resistance rating
This recall involves the Glidescope Go medical device sold in Canada. It's being recalled because a manufacturing variat...
Medical devices• Updated Jan 3
PEDIASAT OXIMETRY CATHETER SET recall in Canada: Interlumen leakage
This recall involves the PEDIASAT OXIMETRY CATHETER SET sold in Canada. It's being recalled because of a manufacturing d...
Medical devices• Updated Jan 3• BHR
BHR SQUARE HEADED NAIL recall in Canada: manufacturing defect
This recall involves BHR SQUARE HEADED NAIL medical devices sold in Canada. They are being recalled because they were ma...
Medical devices• Updated Jan 3• BAYLIS
BAYLIS V4C-560 Ventilator recall in Canada: Safety cannot be assured
This recall involves two units of the BAYLIS V4C-560 Ventilator sold in Canada. It's being recalled because a labeling e...
Medical devices• Updated Jan 3• GORE
GORE Molding and Occlusion Balloon Catheter recall in Canada: Device malfunction
This recall involves the GORE Molding and Occlusion Balloon Catheter sold in Canada. It's being recalled because the dev...
Medical devices• Updated Jan 3• Lyra
Lyra SARS-CoV-2 Assay (M120) recall in Canada: Incorrect test results
This recall involves the Lyra SARS-CoV-2 Assay (M120) sold in Canada. It's being recalled because it may give false nega...
Medical devices• Updated Jan 3• COBAS
COBAS INFINITY CENTRAL LAB recall in Canada: incorrect test results
This recall involves the COBAS INFINITY CENTRAL LAB medical device. It's being recalled because it could provide incorre...
Medical devices• Updated Jan 3• Fabius
Fabius System recall in Canada: New reprocessing instructions
This recall involves Fabius-type anesthesia machines sold in Canada. Draeger is providing new reprocessing instructions
Medical devices• Updated Jan 3• ATTUNE
ATTUNE REVISION CEMENTED STEM recall in Canada: Incorrect size
This recall involves the ATTUNE REVISION CEMENTED STEM 16X80MM sold in Canada. It's being recalled because some packages...
Medical devices• Updated Jan 3
MICRO-FLO, HAEMO-FLO, and MINI-FLO products recall in Canada: infection risk
This recall involves MICRO-FLO, HAEMO-FLO, and MINI-FLO medical devices sold in Canada. They are being recalled because
Medical devices• Updated Jan 3• MUST KIT PLUS
MUST KIT PLUS recall in Canada: Medical device issue
This recall involves MUST KIT PLUS medical devices sold in Canada. They are being recalled due to falsified cycle graphs...
Get Medical devices recall alerts
Receive email alerts when new medical devices recalls are issued in Canada.
Browse other categories
All recallsBrowse by time: