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 0 minutes ago
Canada
Rubicon Holdings Corp. recalls one lot of Simply Bare Organics BC Organic Blue Dream Pre-Rolls due to packaging and labelling issue
The affected products contain the wrong pre-rolls.Gore® Tag® Thoracic Branch Endoprosthesis Side Branch Component
Catheter separation of the Gore® Tag® Thoracic Branch Endoprosthesis (TBE) Side Branch (SB) component during clinical use.WendyLett 4Way
Certain units of WendyLett 4Way, 200 × 190 cm, with handles, may be affected by a material defect that could cause the fabric to tear in or adjacent to the seams.CORFLO* Safety PEG Kit With ENfit® Connector
This recall is initiated due to quality issues related to sterility assurance to certain lidocaine hydrochloride injection products.Red Rubber Latex Catheters
Specific items of Medline Red Rubber Intermittent Catheters have been recalled due to stability testing failure, such as catheter surface finish, connector security.GSP® Neonatal GALT kit
The recall is initiated to inform customers of an observed reduced on-board stability of GSP GALT assay (3303-001U), which may increase the likelihood of delayed…Merlin™ 3650 Patient Care System (PCS)
Abbott is reaching out to customers to inform about a Merlin™ PCS 3650 programmer software update that addresses a software behavior that may occur during Pacing…Kirkland Signature Women 50+ Multivitamin: may contain the presence of foreign matter (metal fragments)
Affected lot may contain the presence of foreign matter (metal fragments).LIFEPAK 15 V4 SpCO/SpMet Sensors
Stryker received complaints indicating that the LIFEPAK 15 V4 displayed an error where “SpO2: Sensor does not support SpCO or SpMET.” The error results in preventing…Cincinnati Surgical Branded Blades And Scalpels
Unlicensed medical devices were sold into Canada - Swann Morton manufactures Cincinnati surgical branded medical devices.Neurological Sponges
During an internal review, Medicom has identified the potential for unexpected variability of endotoxin levels on the products.HarmonyAIR A-Series Surgical Lighting System AND ALYON Surgical Lighting System
Steris identified through customer complaints that on Harmonyair A-Series Lighting System and Alyon Surgical Lighting System the plus/minus (+/-) buttons that control…Honibe Honey Gummies - Melatonin: Daily recommended intake may cause the active ingredient to exceed the allowable limit.
The maximum daily intake may cause the active ingredient to exceed the allowable limit.ERYTHROMYCIN OPHTHALMIC OINTMENT USP: The sterility of the product could be compromised.
The sterility of the product could be compromised in the affected lot.Personnelle Supravite Energizing Formula: The breakage of vials can generate glass fragments
The breakage of vials can generate glass fragments.Exoplan
During internal testing of libraries an error was identified within specific Straumann surgical protocol libraries used with Exoplan version 3.1.
CannaPiece Corp. recalls JAYs - Pink Pennifer 0.4g all-in-one vape due to labelling issue
The label for the affected product has incorrect cannabinoid values.ApexPro Carescape Telemetry Server
Potential loss of ECG and SPo2 monitoring involving ApexPro Carescape Telemetry Server V5.0 and V6.0 can result from a persistent no comm or off network condition at…Hard Disk Drives in Azurion and Allura Systems
Philips has identified that Hard Disk Drives (HDDs) used in the PCS of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond…
Asung Trading Inc. 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.CASE Cardiac Testing System - Parts
Potential for electrical sparking at the printer head of CASE V7 systems.Endoflip System
The issue concerns a problem affecting EF and ES catheters used with EF-100 systems after 1-January-2026.directCHECK™ Whole Blood Control
Instances of consistently elevated results were identified when using directCHECK™ Whole Blood Control DCGLR‑2, lot A6DLA001.A little guidance
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