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 4 minutes ago
Canada
Sanofi-Aventis Canada Inc. recalling certain insulin pens and cartridges
Sanofi-Aventis Canada Inc.Limited number of Sarclisa single use vials may have been frozen during shipment
Units of the affected lot may have been frozen during shipping.Amplatzer™ Amulet™ Left Atrial Appendage Occluder
The current Amulet™ IFU contains a contraindication against use "where placement of the device would interfere with any intracardiac or intravascular structures."…PERMA-HAND™ Silk Suture
Ethicon determined that PERMA-HAND™ Silk Suture subject to this recall (removal) was incorrectly manufactured with an alcohol-based tubing fluid in the primary packaging.Inzone® Detachment System
Stryker has observed that some devices may experience premature battery drain.Likorall™ Patient Lift Systems
Baxter Corporation is issuing an urgent medical device correction for the Likorall™ ceiling-mounted overhead patient lift system due to a potential issue involving…InterStim™ Systems
Medtronic has received 15 complaints involving the selection of an incompatible component based on the intended system configuration between 01-Jan-2020 through…IMAAVY: Affected lots may contain glass particles
Affected lots may contain glass particles.Williams Cystoscopic Injection Needle
Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification.OmniaSecure™ MRI SureScan™
Medtronic’s manufacturing quality processes identified a subset of OmniaSecure™ (Model 3930M) defibrillation leads which may have undergone a specific manufacturing…
Schwarzkopf Professional Osis Grip Mousse recalled due to injury hazard
The recalled product has packaging issues, which can cause the product to leak from the package when under pressure.
Counterfeit laser hair removal and therapy devices found in some clinics and may pose serious health risks
Health Canada is advising Canadians about counterfeit laser hair removal machines and therapy systems sold under the “Soprano” brand.SIGNA™ Artist and SIGNA™ Artist Evo
GE Healthcare has become aware of an exposed sharp edge inside the SIGNA™ Artist Evo and SIGNA™ Artist electronics cabinet that could damage power cables, which may…RAPICIDE™ PA High Level Disinfectant
STERIS identified through customer complaints that a small number of RAPICIDE™ Part A bottles within certain lots may begin to bulge or expand over time.Trinity Biotech Oxalate Reagent Kit
Trinity Biotech is recalling Oxalate Reagent B, Product Code 591-2, Lot 2500711 due to performance variability resulting in negative bias and under-recovery of oxalate…Philips Ingenia, Achieva and Intera MR Systems
When exporting diffusion tensor imaging (DTI) scans from a Philips MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion…IntelliSpace Critical Care And Anesthesia
In ICCA releases J.06.01 and J.06.02, calculations triggered by infusion-pump auto-charting may result in incorrect Intake Totals, Output Totals, Net Body Balance…NDI Passive Spheres™
The sphere manufacturer has identified variation in the reflective material used on a limited number of sterile passive sphere lots.Platinum Naturals Easymulti Stress (men): Affected lots incorrectly labelled for Vitamin B6 quantity
Affected lots are labelled with the incorrect amount of a medicinal ingredient (Vitamin B6).Organika® Gummies: Foreign site not listed on site licence
Affected lots were imported from a foreign manufacturing site not listed on the site licence.
Olli Brands Inc. recalls Olli StikiStix Multipack Sour Razzy Pink Lemonade (300 CBG 100 THC) due to labelling issues
The affected product has multiple labelling issues including missing information.TZIELD (teplizumab) and the Risk of Viral Reactivation
Serious and life-threatening cases of viral reactivation, including Epstein–Barr virus (EBV) and cytomegalovirus (CMV), have been reported with TZIELD.
Generic acetaminophen by Teva recalled because it may contain foreign material
Teva Canada Limited is recalling one lot of the non-prescription drug Novo-Gesic Forte 500 mg (acetaminophen) due to the potential presence of phenolic resin or epoxy…A little guidance
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