Medical devices• Updated Jan 3• Vidas
Vidas products recall in Canada: potential for delayed test results
This recall involves several Vidas Immuno-Assay products used with Vidas Systems in Canada. They are being recalled beca...
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 95 of 220
Medical devices• Updated Jan 3
ORT (2021-09-20)
This recall involves the ORT300 operating room table sold in Canada. It's being recalled because a malfunction in the fl...
Medical devices• Updated Jan 3• MONACO
MONACO recall in Canada: Medical device software issue
This recall involves MONACO medical device software sold in Canada. It's being recalled because contour changes can be s...
Medical devices• Updated Jan 3• AIRO
AIRO MOBILE CT SYSTEM recall in Canada: electrical hazard
This recall involves the AIRO MOBILE CT SYSTEM sold in Canada. It's being recalled because a fuse block may not meet ele...
Medical devices• Updated Jan 3• ARROW-TREROTOLA
ARROW-TREROTOLA OVER-THE-WIRE PTD KIT recall in Canada: inner lumen may detach
This recall involves the ARROW-TREROTOLA OVER-THE-WIRE PTD KIT sold in Canada. It's being recalled because the device's
Medical devices• Updated Jan 3• SPIROS
SPIROS CLOSED MALE LUER recall in Canada: Leaking hazard
This recall involves certain lots of SPIROS CLOSED MALE LUER medical devices sold in Canada. They are being recalled bec...
Medical devices• Updated Jan 3
Automated Field Steam Sterilizer recall in Canada: Electrical shock risk
This recall involves the Automated Field Steam Sterilizer sold in Canada. It's being recalled because a part of the devi...
Medical devices• Updated Jan 3• Cardiosave System
Cardiosave System - Battery Only recall in Canada: battery may fail
This recall involves the Cardiosave System - Battery Only sold in Canada. It's being recalled because the battery pack m...
Medical devices• Updated Jan 3• ROSA One
ROSA One 3.1 Brain recall in Canada: Inaccurate electrode placement
This recall involves the ROSA One 3.1 Brain application system sold in Canada. It's being recalled because a software an...
Medical devices• Updated Jan 3• Trutest
Trutest Closed Suction System recall in Canada: ventilation interruption risk
This recall involves the Trutest Closed Suction System Double Swivel Elbow Adult 72 hours Endotracheal, a medical device...
Medical devices• Updated Jan 3
Graphene face masks recall in Canada: potential lung effects
This recall involves certain face masks labelled to contain graphene or biomass graphene sold in Canada. They are being
Medical devices• Updated Jan 3• Chesapeake
Chesapeake Anterior Lumbar Removal Tool recall in Canada: missing pins
This recall involves the Chesapeake Anterior Lumbar Removal Tool sold in Canada. It's being recalled because some units
Medical devices• Updated Jan 3• Atellica
Atellica IM Analyzer recall in Canada: inaccurate test results
This recall involves Atellica IM 1300 and Atellica IM 1600 Analyzers sold in Canada. They are being recalled because the...
Medical devices• Updated Jan 3• CARDIOSAVE SYSTEM
CARDIOSAVE SYSTEM recall in Canada: Device malfunction risk
This recall involves the CARDIOSAVE SYSTEM - HYBRID & RESCUE INTRA-AORTIC BALLOON PUMP sold in Canada. It's being recall...
Medical devices• Updated Jan 3• NEOFEED
NEOFEED ENTERAL SYRINGE PUMP recall in Canada: under infusion risk
This recall involves the NEOFEED ENTERAL SYRINGE PUMP sold in Canada. It's being recalled because the pump mechanism can...
Medical devices• Updated Jan 3• Atrium
Pneumostat Chest Drain Valve recall in Canada: patient risk
This recall involves the Atrium Pneumostat Chest Drain Valve sold in Canada. It's being recalled because the instruction...
Medical devices• Updated Jan 3
Instrument Manager recall in Canada: Incorrect timestamp readings
This recall involves the Instrument Manager software sold in Canada. It's being recalled because it may not read timesta...
Medical devices• Updated Jan 3• ALINITY M
ALINITY M SARS AMP KIT recall in Canada: False positive results
This recall involves the ALINITY M SARS-COV-2 AMP KIT and ALINITY M RESP-4 PLEX AMP KIT sold in Canada. They are being r...
Medical devices• Updated Jan 3
Lightweight CABRIO Cable recall in Canada: Erroneous labeling
This recall involves Lightweight CABRIO Cable medical devices sold in Canada. It's being recalled because of erroneous l...
Medical devices• Updated Jan 3• DLP
DLP Left Heart Vent Catheters recall in Canada: labeling error
This recall involves DLP Left Heart Vent Catheters, 16 Fr, sold in Canada. It's being recalled because of erroneous labe...
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