Medicine, medical device and cosmetics recalls in Canada
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in Canada, newest first.
664 recalls, newest first · Checked 19 minutes ago
CanadaUltraview SL™ Command Module
It was discovered during production testing that the cardiac output function of the multiparameter module model 91496 was intermittently yielding bad or irregular curves.B. Braun Hemodialysis Blood Tubing Set
The potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.Auro-Canagliflozin: Affected lots are labelled with the incorrect DIN found on the blister card.
Affected lots are labelled with the incorrect DIN found on the blister card.LUXA-D: A capsule containing a foreign product was found in the affected batch.
A capsule containing a foreign product was found in the affected batch.Moxifloxacin : assay out of trend
The assay is out of trend in the affected lot.Cardinal Health Cardiac Electrophysiology (EP) Packs
Cardinal Health was recently informed of a medical device recall from Medline Industries.Medline Namic Angiographic Control Syringes
The Namic RA syringes have been recalled by Medline due to a potential risk of the syringe rotating adaptor unwinding during use.HIZENTRA: The appearance is out of specification in the affected lot.
The appearance is out of specification in the affected lot.
Unauthorized and counterfeit health products seized at Thumbs Up 4 Shiatsu in Mississauga may pose serious health risks
Health Canada is warning consumers about multiple unauthorized and counterfeit health products seized at Thumbs Up 4 Shiatsu in Mississauga, Ontario.Olympus HF Cable
Olympus received a complaint involving a thermal event with an HF cable during a procedure, causing a user burn.iVascular Navitian
A potential risk has been identified through post-market surveillance: deterioration of the outer layer of the thinner distal segment of the device, which could lead to…Ortho Connect
A potential safety issue was reported of incorrectly releasing discrepant test results to a healthcare environment identified under very specific conditions.UniCel DxI 600 Access Immunoassay System-Total T4 Assay
Access Total T4 calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product specifications.Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.Vacuum Bag SU Large
Leakage from the specimen container may occur.Soft-Vu and Accu-Vu 4 FR Angiographic Catheters
AngioDynamics, Inc., is conducting a voluntary medical device field safety corrective action or recall to the end-user level based on the non-conformance of a molded…Disinfectant Spray & Wipe Cleaner: Affected lots contain solution that do not meet the labelled strength
Affected lots contain solution that do not meet the labelled strength.Allura Xper and Azurion Systems
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch due to: cable or connector damage…Olympus Medical PK/PKS/Everest Cutting Forceps
Olympus identified inadequate supplier welding validation on several 5 mm cutting forceps models, which may cause jaw breakage during clinical use.RAPIDPoint® 500 Blood Gas Systems
Siemens Healthineers has confirmed that a limited number of Measurement Cartridge experienced exposure to temperatures below the specified storage conditions during…Approach® CTO Micro Wire Guide, Blue Rhino® G2-Multi Percutaneous Tracheostomy Introducer Set, Wayne Pneumothorax Set, Cook Spectrum® Central Venous Catheter Sets
Devices from the affected device lots have labels that state the incorrect expiration dates.GEM PAKs for the GEM Premier 5000 with iQM2
The company confirmed customer complaints indicating that specific GEM PAKs (cartridges) for the Gem Premier 5000 may experience an increased incidence of "Process…
Clore Beauty Supply products recalled due to missing mandatory hazard labelling
The recalled products do not have mandatory hazard labelling as required by the Cosmetic Regulations under the Food and Drugs Act, or the Consumer Chemical and…A little guidance
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