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 13 minutes ago
CanadaAptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay Software
This notification is to inform Panther and Panther Fusion users that assay installer (version 2.0.0.9) including the Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and…Selenia Dimensions 2D/3D Mammography Systems
Hologic is initiating this voluntary field safety corrective action because the vertical travel assembly on 3Dimensions and Selenia Dimensions systems may experience…Nicotine Pouch Recall; No market authorization
Product sold without market authorization (DIN) in Canada.
CannaPiece Corp. recalls Wild West 96+ Strawberry Stampede Liquid Diamonds 510 Vape due to a labelling issue
The label for the affected product has incorrect cannabinoid values.Guedel Airway
During manufacture, some devices have been identified with occluded or partially occluded tips of the Guedel Airway.PMS-Fluconazole 50 mg tablets; Incorrect quantity of tablets
The affected batch may not contain the correct quantity of tablets.Baxter Corporation products recall; Blue cap breakage
Blue Caps Enhanced Closures (blue tip protectors) may break apart in affected lots.
Renpure Tea Tree & Rosemary Scalp Rebalancing Shampoo & Conditioner recalled due to microbial contamination
These lot codes have elevated microbial levels including aerobic bacteria count, yeast/mold count and Burkholderia cepacia complex which may cause irritation and…Harmony™ Delivery Catheter System
Medtronic had received two (2) complaints about Harmony™ DCS distal tip detachment during the implant procedure.Philips Allura Xper Systems
Under certain conditions, the hand switch button may not fully release after being pressed, potentially resulting in loss of imaging functionality or unintended…Giraffe™ OmniBed™ Carestation™
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device.ARTIS Icono Ceiling, Floor and Biplane Systems
In very rare situations, after increasing the detector lift height to its maximum or minimum, the system may lose its movement capability.Dexcom G7 Sensor 1 Pack
Unauthorized third-party distribution of 2 Dexcom G7 sensor lots in Canada that were intended for destruction as they did not meet Dexcom product standardsIntelliCuff®
An issue was identified where the affected IntelliCuff® devices may alarm with "cuff system leakage", the motor pumps continuously and does not maintain the cuff…BD Canada ChloraPrep product recall; Sterility concerns
Product sterility is compromised in affected lots.IceMan CLASSIC3™
Complaints received reporting a consistent failure mode described as a broken connector on IceMan CLASSIC™ cube unit.
Hybrid Infusions Ltd. recalls Champagne Supernova 3x0.5g Pre-Roll due to packaging and labelling issue
The affected product is packaged in the wrong tube.Hizentra: The appearance is out of specification in the affected lot.
The appearance is out of specification in the affected lot.Relay®Pro Thoracic Stent-Graft System
Through post-market surveillance, Bolton Medical received complaints where the graft is unable to unclasp from the delivery system because the proximal clasp is…CRE™ Wireguided and CRE PRO™ Wireguided Balloon Dilation Catheters
Boston Scientific is initiating removal of CRE™ Wireguided and CRE PRO™ Wireguided balloon dilation catheters due to a potential sterile breach of the pouches in which…Volara System Patient Ciruit
Baxter Corporation is issuing an urgent medical device correction for Volara System patient circuits due to reports of air and medication leakage from the nebulizer cup…Omnipod® Insulin Management System - Omnipod®
The defect is related to tears on the external (exposed) soft cannula.GE Healthcare AW Server
Potential patient context synchronization issue.A little guidance
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