Medical devices• Updated Jan 3
Transseptal Needle Sets recall in Canada: Rust contamination
This recall involves Transseptal Needle Sets sold in Canada. They are being recalled because they may contain rust on th...
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 94 of 220
Medical devices• Updated Jan 3• VACUETTE
VACUETTE 2 ml K2 EDTA recall in Canada: Inaccurate test results
This recall involves VACUETTE 2 ml K2 EDTA blood collection tubes sold in Canada. They are being recalled because they m...
Medical devices• Updated Jan 3• Welch Allyn
ELI280 Resting Electrocardiograph recall in Canada: software fault
This recall involves the ELI280 Resting Electrocardiograph sold in Canada. It's being recalled because a software fault
Medical devices• Updated Jan 3• PRISMAX
PRISMAX CONTROL UNIT recall in Canada: incorrect display of prescription values
This recall involves the PRISMAX CONTROL UNIT sold in Canada. It's being recalled because it may display incorrect presc...
Medical devices• Updated Jan 3• AZURION
AZURION products recall in Canada: Medical device malfunction risk
This recall involves AZURION 7 M12, AZURION 7 M20, and AZURION 7 B12 products sold in Canada. They are being recalled be...
Medical devices• Updated Jan 3
MS-12 BLUE, CARDIOVIT CS-200 Office recall in Canada: incorrect diagnosis risk
This recall involves the MS-12 BLUE, CARDIOVIT CS-200 Office medical device sold in Canada. It's being recalled because
Medical devices• Updated Jan 3• Supercore
Supercore instruments recall in Canada: May come apart
This recall involves Supercore II and Supercore Biopsy Instrument with Co-axial Introducer Needle Kit sold in Canada. It...
Medical devices• Updated Jan 3• EMBLEM
EMBLEM S-ICD Subcutaneous Electrode recall in Canada: fracture risk
This recall involves the EMBLEM S-ICD Subcutaneous Electrode sold in Canada. It's being recalled because the electrode m...
Medical devices• Updated Jan 3
LEEP PRECISION GENERATOR recall in Canada: bleeding risk
This recall involves the LEEP PRECISION GENERATOR, a medical device used in Canada. It's being recalled because it may f...
Medical devices• Updated Jan 3
Stem-Kit Reagents recall in Canada: May lead to erroneous results
This recall involves Stem-Kit Reagents sold in Canada. It's being recalled because incorrect instructions for use may le...
Medical devices• Updated Jan 3
S.M.A.R.T. FLEX BILIARY STENT SYSTEM recall in Canada: Tip dislodgement
This recall involves the S.M.A.R.T. FLEX BILIARY STENT SYSTEM sold in Canada. It's being recalled because inadequate adh...
Medical devices• Updated Jan 3• Simplexa
Simplexa COVID-19 Positive Control Pack recall in Canada: invalid results
This recall involves the Simplexa COVID-19 Positive Control Pack sold in Canada. It's being recalled because it may prod...
Medical devices• Updated Jan 3
N95 Particulate Respirator recall in Canada: NIOSH certification revoked
This recall involves N95 Particulate Respirators (models DTC3B, DTC3M-1, DTC3W, DTC3X, DTC3Z) sold in Canada. It's being...
Medical devices• Updated Jan 3• MiniMed
MiniMed 600 series recall in Canada: Insulin delivery risk
This recall involves MiniMed 600 series insulin pumps sold in Canada. It's being recalled because a damaged retainer rin...
Medical devices• Updated Jan 3
N95 Particulate Respirator recall in Canada: NIOSH certification revoked
This recall involves N95 Particulate Respirators (models DTC3Z, DTC3B, DTC3W, DTC3M-1) sold in Canada. It's being recall...
Medical devices• Updated Jan 3• Elekta Limited
Elekta Limited Digital Accelerators recall in Canada: injury risk
This recall involves several models of Elekta Limited Digital Accelerators used in medical settings in Canada. They are
Medical devices• Updated Jan 3• Biomeme
Biomeme SARS-CoV-2 Real-Time RT-PCR Test recall in Canada: Unapproved software
This recall involves the Biomeme SARS-CoV-2 Real-Time RT-PCR Test sold in Canada. It's being recalled because an unappro...
Medical devices• Updated Jan 3
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM recall in Canada: software issue
This recall involves the EPIQ DIAGNOSTIC ULTRASOUND SYSTEM sold in Canada. It's being recalled because a software issue
Medical devices• Updated Jan 3• Rusch
Rusch Endotracheal Tube recall in Canada: inflation issue
This recall involves various Rusch Endotracheal Tubes sold in Canada. They are being recalled because the tube cuff coul...
Medical devices• Updated Jan 3• Bodyguard
Bodyguard pumps recall in Canada: risk of under-infusion
This recall involves Bodyguard Twins and Bodyguard 323 IV Infusion Pumps sold in Canada. They are being recalled because...
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