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VERIFIED OFFICIAL-SOURCE INDEX

Current Product Recalls in Canada – Page 5

Browse official recall notices for Canada, then compare the product and every listed identifier with the item you own.

Last updated: October 10, 2026 at 1:40 AM UTC · Official sources are checked throughout the day.

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344 current and recent recalls

Showing 161–200 of 344 notices · Page 5 of 9

Health Canada · September 4, 2026

LIFEPAK ® 35 Monitor/Defibrillator Recall: During production of LP35, Stryker identified that

Affected product
LIFEPAK ® 35 Monitor/Defibrillator
Category
Medical device recalls
Hazard
During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut…
Check affected LIFEPAK ® 35 Monitor/Defibrillator identifiers →

Health Canada · September 4, 2026

LIFEPAK ® 35 Monitor/Defibrillator Recall: During production of LP35, Stryker identified that

Affected product
LIFEPAK ® 35 Monitor/Defibrillator
Category
Product recall
Hazard
During production of LP35, Stryker identified that certain printer and modem access port connectors may not have been fully seated within the rear housing assembly. As a result, the connectors may appear flush with or recessed relative to the retaining nut…
Check affected LIFEPAK ® 35 Monitor/Defibrillator identifiers →

Transport Canada · September 4, 2026

NOVA BUS issued a on the LFS model Recall: could cause the control unit to shut down

Affected product
NOVA BUS issued a on the LFS model
Category
Vehicle recalls
Hazard
could cause the control unit to shut down. If this happens, there could be a sudden loss of power to the wheels. Note: This recall replaces Transport Canada recall no. 2026-220 Safety Risk: A loss of power to the wheels could increase the risk of a crash. A…
Check affected NOVA BUS issued a on the LFS model identifiers →

Government of Canada Consumer Product Safety · September 3, 2026

DUNLOP RigPro full safety boots recalled electric shock hazard Recall: Brand(s) DUNLOP Last updated

Affected product
DUNLOP RigPro full safety boots recalled electric shock hazard
Category
Consumer product recalls
Hazard
Brand(s) DUNLOP Last updated 2026-09-03 Summary Product Dunlop RigPro full safety Boots Issue Consumer products - Electrical hazard What to do Immediately stop using the recalled product and return it for a refund. Distribution National Previous Next
Check affected DUNLOP RigPro full safety boots recalled electric shock hazard identifiers →

Government of Canada Consumer Product Safety · September 3, 2026

Amana Through the Wall (TTW) air conditioners or heat pumps recalled Recall: Brand(s) Amana Last updated

Affected product
Amana Through the Wall (TTW) air conditioners or heat pumps recalled
Category
Consumer product recalls
Hazard
Brand(s) Amana Last updated 2026-09-03 Summary Product Amana Through the Wall (TTW) air conditioners or heat pumps Issue Consumer products - Fire hazard What to do Immediately stop using the recalled product and
Check affected Amana Through the Wall (TTW) air conditioners or heat pumps recalled identifiers →

Government of Canada Consumer Product Safety · September 3, 2026

Branch Ergonomic Chairs recalled fall hazard Recall: Brand(s) Branch Last updated 2026-09-03 Summary

Affected product
Branch Ergonomic Chairs recalled fall hazard
Category
Consumer product recalls
Hazard
Brand(s) Branch Last updated 2026-09-03 Summary Product Ergonomic Chairs Issue Consumer products - Fall hazard What to do Immediately stop using the recalled product and
Check affected Branch Ergonomic Chairs recalled fall hazard identifiers →

Transport Canada · September 3, 2026

NOVA BUS issued a on the LFS, and LFS ARTIC models Recall: A sudden loss of power to the wheels could

Affected product
NOVA BUS issued a on the LFS, and LFS ARTIC models
Category
Vehicle recalls
Hazard
A sudden loss of power to the wheels could increase the risk of a crash. A bus that is disabled could result in a transfer of passengers in an uncontrolled environment, which may create a risk of injury. Corrective Actions: Nova Bus will notify owners by mail…
Check affected NOVA BUS issued a on the LFS, and LFS ARTIC models identifiers →

Transport Canada · September 3, 2026

TIFFIN issued a on the WAYFARER model Recall: If there is a propane leak and there is no remote

Affected product
TIFFIN issued a on the WAYFARER model
Category
Vehicle recalls
Hazard
If there is a propane leak and there is no remote shut-off valve, there could be an increased risk of a fire or explosion. Additionally, a propane tank that detaches from the motorhome could create a road hazard for others and increase the risk of a crash.…
Check affected TIFFIN issued a on the WAYFARER model identifiers →

Health Canada · September 2, 2026

LIFEPAK ® 35 Monitor/Defibrillator Recall: Stryker has identified an issue with the LP35 where

Affected product
LIFEPAK ® 35 Monitor/Defibrillator
Category
Product recall
Hazard
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific conditions are present simultaneously. The issue does not affect the display of "shock advised" or…
Check affected LIFEPAK ® 35 Monitor/Defibrillator identifiers →

Health Canada · September 2, 2026

BiCOAG Hemostasis Probe Recall: Olympus determined that the affected products may

Affected product
BiCOAG Hemostasis Probe
Category
Medical device recalls
Hazard
Olympus determined that the affected products may have been manufactured without the designated amount of adhesive to the rear of the device’s ceramic tip, which may result in detachment of the ceramic tip. Customers should immediately discontinue using the…
Check affected BiCOAG Hemostasis Probe identifiers →

Health Canada · September 2, 2026

LEO+ Intracranial Self Expandable Stent And Delivery System Recall: As a precautionary measure, Balt

Affected product
LEO+ Intracranial Self Expandable Stent And Delivery System
Category
Medical device recalls
Hazard
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial endotoxin test results. The recall affects both standalone ANRYV connectors and ANRYV connectors…
Check affected LEO+ Intracranial Self Expandable Stent And Delivery System identifiers →

Transport Canada · September 2, 2026

TOYOTA issued a on the C-HR model Recall: in the battery electric vehicle control unit (BEV

Affected product
TOYOTA issued a on the C-HR model
Category
Vehicle recalls
Hazard
in the battery electric vehicle control unit (BEV ECU) could cause the electric drive system to shut down while driving. If this happens, there could be a sudden loss of power to the wheels. Safety Risk: A sudden loss of power to the wheels could increase the…
Check affected TOYOTA issued a on the C-HR model identifiers →

Transport Canada · September 2, 2026

YAMAHA issued a on the YAMAHA CROSSWAVE TRAILER (YAB16SESALT0), and Recall: Poor handling or a tire failure

Affected product
YAMAHA issued a on the YAMAHA CROSSWAVE TRAILER (YAB16SESALT0), and
Category
Vehicle recalls
Hazard
Poor handling or a tire failure could cause a loss of vehicle control and result in a crash. Corrective Action: Yamaha will notify owners by mail and advise you to
Check affected YAMAHA issued a on the YAMAHA CROSSWAVE TRAILER (YAB16SESALT0), and identifiers →

Health Canada · September 2, 2026

Quantum PureFlow Standard Heat Exchanger High Flow Recall: Blood-to-glycol leakage was identified in the

Affected product
Quantum PureFlow Standard Heat Exchanger High Flow
Category
Medical device recalls
Hazard
Blood-to-glycol leakage was identified in the heat exchanger during the procedure. Glycol compartment contamination may result in blood contamination of the heater-cooler due to glycol circulation for thermoregulation. Customer communication is considered…
Check affected Quantum PureFlow Standard Heat Exchanger High Flow identifiers →

Canadian Food Inspection Agency · September 1, 2026

Coaticook brand Aged Cheddar Cheese recalled Listeria monocytogenes Recall: Although infected pregnant women

Affected product
Coaticook brand Aged Cheddar Cheese recalled Listeria monocytogenes
Category
Food recalls
Hazard
Although infected pregnant women may experience only mild, flu-like symptoms, the infection can lead to premature delivery, infection of the newborn or even stillbirth. In severe cases of illness, people may die. Learn more: Learn more about the health risks…
Check affected Coaticook brand Aged Cheddar Cheese recalled Listeria monocytogenes identifiers →

Transport Canada · September 1, 2026

FOREST RIVER issued a on the VIBE model Recall: A build-up of exhaust gas in the trailer could

Affected product
FOREST RIVER issued a on the VIBE model
Category
Vehicle recalls
Hazard
A build-up of exhaust gas in the trailer could result in carbon monoxide poisoning. Corrective Actions: To reduce the safety risk, Forest River recommends not using the furnace until recall repairs have been completed. Forest River will notify the owner by…
Check affected FOREST RIVER issued a on the VIBE model identifiers →

Transport Canada · September 1, 2026

FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CARAVAN, and Recall: with the brake pedal position sensor

Affected product
FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CARAVAN, and
Category
Vehicle recalls
Hazard
with the brake pedal position sensor could cause the electronic stability control (ESC) system not to work. Note: This problem would cause the electronic stability control (ESC) warning light to turn on. Safety Risk: An electronic stability control system that…
Check affected FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CARAVAN, and identifiers →

Transport Canada · September 1, 2026

FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CHEROKEE model Recall: A coil spring that detaches from the

Affected product
FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CHEROKEE model
Category
Vehicle recalls
Hazard
A coil spring that detaches from the vehicle could create a road hazard for others and increase the risk of a crash. Corrective Actions: FCA Canada will notify owners in writing and advise you to take your vehicle to a dealership to replace the rear coil…
Check affected FIAT CHRYSLER AUTOMOBILES issued a on the GRAND CHEROKEE model identifiers →

Transport Canada · September 1, 2026

FIAT CHRYSLER AUTOMOBILES issued a on the 1500 model Recall: could cause the rearview camera not to display

Affected product
FIAT CHRYSLER AUTOMOBILES issued a on the 1500 model
Category
Vehicle recalls
Hazard
could cause the rearview camera not to display when the transmission is shifted into reverse. Canadian regulations require the rearview image to display when the vehicle is reversing. Safety Risk: A rearview camera image that doesn't display could reduce a…
Check affected FIAT CHRYSLER AUTOMOBILES issued a on the 1500 model identifiers →

Transport Canada · September 1, 2026

PACCAR issued a on the 548 model Recall: Brakes that take too long to apply and/or that

Affected product
PACCAR issued a on the 548 model
Category
Vehicle recalls
Hazard
Brakes that take too long to apply and/or that release too slowly could increase the risk of a crash. Corrective Actions: PACCAR will notify owners by mail and advise you to take your truck to a dealership to replace the front brake valve. The dealer will also…
Check affected PACCAR issued a on the 548 model identifiers →

Transport Canada · August 31, 2026

JAYCO issued a on the SENECA PRESTIGE MOTORHOME, SENECA MOTORHOME Recall: Poor handling or a tire failure

Affected product
JAYCO issued a on the SENECA PRESTIGE MOTORHOME, SENECA MOTORHOME
Category
Vehicle recalls
Hazard
Poor handling or a tire failure could cause a loss of control and increase the risk of a crash. Corrective Actions: Jayco will mail a new compliance label to each owner. If you'd like help to install the label, you can
Check affected JAYCO issued a on the SENECA PRESTIGE MOTORHOME, SENECA MOTORHOME identifiers →

Health Canada · August 28, 2026

Blanketrol® II 115V and Blanketrol® III 115V Recall: Gentherm Medical has received complaints of

Affected product
Blanketrol® II 115V and Blanketrol® III 115V
Category
Product recall
Hazard
Gentherm Medical has received complaints of overheated circuit boards in 0.53% of distributed devices. Overheating can cause the circuit board to stop operating, which may result in a device that shuts down at startup or during use on a patient. Based on the…
Check affected Blanketrol® II 115V and Blanketrol® III 115V identifiers →

Transport Canada · August 27, 2026

POLARIS issued a on the RANGER XP 1000, and RANGER XP 1000 CREW Recall: Missing safety information could

Affected product
POLARIS issued a on the RANGER XP 1000, and RANGER XP 1000 CREW
Category
Vehicle recalls
Hazard
Missing safety information could create an increased risk of injury. Corrective Actions: To reduce the safety risk, if the labels have detached, Polaris advises you to consult the safety information in the owner's manual. As an interim repair, Polaris will…
Check affected POLARIS issued a on the RANGER XP 1000, and RANGER XP 1000 CREW identifiers →

Transport Canada · August 27, 2026

GENERAL MOTORS issued a on the CANYON, and COLORADO models Recall: This small error does not affect safety

Affected product
GENERAL MOTORS issued a on the CANYON, and COLORADO models
Category
Vehicle recalls
Hazard
This small error does not affect safety. Corrective Actions: This is not a recall. General Motors has made changes to ensure that all new vehicles meet Canadian regulations. Make Model Model Year(s) Affected CHEVROLET COLORADO 2024 2025 2026 GMC CANYON 2024…
Check affected GENERAL MOTORS issued a on the CANYON, and COLORADO models identifiers →

Health Canada · August 27, 2026

Automated Impella Controller (AIC) Recall: based strategy for component replacement will be

Affected product
Automated Impella Controller (AIC)
Category
Medical device recalls
Hazard
based strategy for component replacement will be implemented. The purge flag is the component that engages with the purge disc and allows the AIC to recognize the purge disc. These AIC purge flag component failures may result most frequently in user…
Check affected Automated Impella Controller (AIC) identifiers →

Health Canada · August 27, 2026

Cardinal Health Gynaecology Robotics and Endoscopy Packs Recall: Cardinal Health was recently informed of a

Affected product
Cardinal Health Gynaecology Robotics and Endoscopy Packs
Category
Medical device recalls
Hazard
Cardinal Health was recently informed of a medical device recall from Stryker concerning the StrykeFlow PS referenced. the recall is being issued due to an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Check affected Cardinal Health Gynaecology Robotics and Endoscopy Packs identifiers →

Health Canada · August 27, 2026

pro+ Flat Deck Wide W/O X-Ray Recall: The UDI label for model p7924a13 incorrectly states

Affected product
pro+ Flat Deck Wide W/O X-Ray
Category
Product recall
Hazard
The UDI label for model p7924a13 incorrectly states the product description as "Pro+ 40 MRS surface with x-ray" instead of the actual configuration, which is "Pro+ 36 MRS surface." Model p7924a13 should be used with 36" width bed frames and not 40" width bed…
Check affected pro+ Flat Deck Wide W/O X-Ray identifiers →

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