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 21 minutes ago
CanadaTrilogy EVO and EV300
Philips Respironics prohibits the use of non-pneumatic (e.g., vibrating mesh) nebulizers (FSN 2025-CC-SRC-020) with Trilogy EVO platform ventilators (including Trilogy…Medihoney® Wound and Burn Products
Sterile products: During an investigation, packaging failures were identified related to the Medihoney® wound & burn products, which could lead to a breach in the…Medline Kits containing Surgical Gowns, Packs and Drapes
Medline identified calibration issues linked to the equipment used to sterilize the recalled products, impacting the sterility assurance level.Alphenix Systems
An internal error would occur if F-STORE or image acquisition is performed while CAAS clinical analysis function is used.VISERA™ Imaging System
Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of MAJ-210 and MAJ-1218.TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
Affected lots were manufactured using an active ingredient that was out of specification for dissolution.Cefazolin for Injection: Affected lots are packaged with the incorrect Linear barcode on inner and outer bag labels.
Affected lots are packaged with the incorrect Linear barcode on inner and outer bag labels.MAR-AMLODIPINE: affected lots may contain tablet(s) of Midodrine 2.5mg tablets.
Affected lots may contain tablet(s) of Midodrine 2.5mg tablets.
Two lots of MAR-Amlodipine 5 mg tablets recalled as some bottles may contain the wrong drug
Marcan Pharmaceuticals Inc.UHI-3 High Flow Insufflation System - Insufflator
Olympus is initiating a Medical Device Recall on the High Flow Insufflation Unit Models UHI, UHI-2, UHI-3, and UHI-E.Centricity™ Universal Viewer Zero Footprint Client
Centricity™ Universal Viewer Zero Footprint Client (ZFP) patient timeline may launch incorrect patient.DxC 700 AU and AU5800 Clinical Chemistry Analyzers
Beckman Coulter has determined that some DxC 700 AU and AU5800 Clinical Chemistry Analyzers may unexpectedly generate some errors due to Microsoft® SQL Server® 2022…cobas® pro and cobas® pure
A rare software malfunction has been identified on the cobas® pro (c503) and cobas® pure (c303) platforms affecting the calibration library.EVIS EXERA III Duodenovideoscope
Olympus has updated the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing.Surgical Drapes, Packs, Gowns
Medline identified calibration issues linked to the equipment used to sterilize the recalled products, impacting the sterility assurance level.Medihoney® Wound & Burn Products
During an investigation by the manufacturer, packaging failures were identified related to the Medihoney® Wound & Burn Products, which could lead to a breach in the…Infant/Child Reduced Energy Defibrillation Electrode
On November 21, 2024 Stryker began investigating product complaints related to the gel delamination of pediatric electrodes.CleverCut and FlowCut Sphincterotomes
CleverCut and FlowCut sphincterotome devices which did not undergo thermoforming could deform and lose performance.MOLLI 2 Systems
Stryker has updated the MOLLI 2 system Instructions for Use (IFU) following two medical device reports (MDRs) submitted to the FDA (June 5 2025).Bard Marquee 12g X 10 cm
In September 2024, BD initiated a field action for specific lots of the Marquee™ Disposable Core Biopsy Instruments that were potentially manufactured missing the…OES Pro Urology Resection Sheaths
Further to the FY25-022 medical device recall issued in October 2024, Olympus is informing users of a voluntary product recall action for cystoscope outer sheath.Thinking about buying GLP-1 drugs like Ozempic or Mounjaro? Beware of fake or unauthorized products
With growing interest in GLP-1 products such as semaglutide (e.g.Hemodialysis Opening (Hemodialyse Ouverture) Packs
Cardinal Health was recently informed of a medical device recall from ICU Medical Inc.A little guidance
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