Medicine, medical device and cosmetics recalls in Canada
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in Canada, newest first.
662 recalls, newest first · Checked 10 minutes ago
CanadaDxc 500i Clinical Analyzer and Dxc 500 AU Clinical Chemistry Analyzer
Beckman Coulter identified a software issue affecting DxC 500i and DxC 500 AU Analyzers when testing plasma samples.IMN Screws System Advanced Locking Screw
Following a product complaint, and as part of its standard quality process, Stryker confirmed that one lot of T2 Alpha IMN advanced locking is incorrectly labeled.Veradius Unity and BV Pulsera Mobile C-Arm System-9in. and 12in. Versions
Air bubbles may develop in the monoblock oil when there is a prolonged period between manufacture and installation, for example due to storage, transportation, or other…Philips Ingenia, Achieva and Intera MR Systems
Philips has become aware of a software issue affecting Philips Magnetic Resonance (MR) imaging systems operating with software versions R5 & R11, which may terminate an…LIFEPAK ® 35 Monitor/Defibrillator
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.GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
Gore has identified through quality control testing that some VIABAHN® devices were processed using equipment that was functioning outside of the validated range.
Traditional Kohl Products recalled due to chemical hazard
The recalled products contain lead above the impurity limits outlined in the Guidance on Heavy Metal Impurities in Cosmetics.Imager™ II Angiographic Catheter
Boston Scientific is initiating removal of Imager II Angiographic Catheters (“Catheters”) due to a manufacturing issue affecting the catheter tip.LEO+ Intracranial Self Expandable Stent And Delivery System
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial…LIFEPAK ® 35 Monitor/Defibrillator
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…BiCOAG Hemostasis Probe
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…Quantum PureFlow Standard Heat Exchanger High Flow
Blood-to-glycol leakage was identified in the heat exchanger during the procedure.JAMP Temozolomide: Out-of-Specification (Assay)
The active ingredient (temozolomide) is out of specification in the affected lot.Carestation 850
Unexpected shutdown of Carestation 850 and 850C anesthesia systems when AC mains power is disconnected or AC mains power is lost.Semaglutide Injection : Out-of-Specification (Impurity)
An impurity is out of specification in all lots of the affected products.Apo-Semaglutide Injection : Incorrect dose display
The affected lot may display a 2 mg dose in the dose window and deliver a 2 mg dose instead of the expected 0.25 mg or 0.5 mg dose.Automated Impella Controller (AIC)
Abiomed has initiated a voluntary medical device recall (removal) after identification of an increase in complaints related to purge cassette recognition issues due to…Cardinal Health Gynaecology Robotics and Endoscopy Packs
Cardinal Health was recently informed of a medical device recall from Stryker concerning the StrykeFlow PS referenced.pro+ Flat Deck Wide W/O X-Ray
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…CARESCAPE Central Station
GE Healthcare has become aware that the CARESCAPE Central Station (CSCS) v3.0.x may not resume patient monitoring for at least 3 minutes following a system restart.BIOFIRE® Joint Infection Panel – 30 Pack
Beginning April 5, 2026, elevated rates of KPC unexpected positives were observed in reagent final QC testing of the BIOFIRE® FILMARRAY® Pneumonia Panel, BIOFIRE®…Med-Rx Medication/Primary Solution Administration Kit
CHS was notified by ICU Medical Canada that they are conducting a recall of certain IV sets as discoloration may be present in the drip chamber of the IV sets.Cyanosure DermaV Laser System
Cynosure Lutronic has identified a adverse trend of complaint reports in North America for spark and loud noise resulting in patient burns during vascular treatment…A little guidance
Get more from your tools
Practical guide 3 min read
Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
Practical guide 3 min read
How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
Practical guide 3 min read
What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.