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 4 minutes ago
CanadaMazor™ X System
Mazor software version 5.2 is an update to any prior software version, including software versions 5.0.1, 5.1.2, and 5.1.3.
BEB Bubbly Wash recalled due to microbial contamination
The recalled products can contain the bacteria Klebsiella aerogenes.Rifton TRAM and E-Pacer
Rifton initiated recalls for TRAM and E-Pacer units due to an unrelated buckle spring failure, which led to replacing the full body support strap assembly.Azurion R3.0 Systems
Philips has identified nine software issues affecting Azurion R3.0 systems that may result in loss of imaging (X-ray) functionality, and/or loss of motorized movement…Achieva 3.0T MRI System-Main Unit
Philips has become aware through in-house testing of a potential safety issue affecting MR systems operating on software versions R11.1 to R12.1 that could pose a risk…Teva-Topilene Ointment 0.05%: The assay is potentially out of specification in the affected lot during its shelf life.
The assay is potentially out of specification in the affected lot during its shelf life.Viazen Immunity: The selenium content is out of specification in the affected batch.
The (selenium) content is out of specification in the affected batch.
Mira Henna Cones recalled due to chemical hazard
The recalled products contain phenol which is a prohibited Hotlist ingredient.Sentinel V11 (Sentinel Cardiology Information Managment System)
Spacelabs Healthcare identified two issues with version 11.6.0 that can result in incorrect patient data being associated with clinical reports, potentially resulting…IMRIS HFD100 Head Fixation Device
IMRIS is conducting a voluntary recall to address a potential safety risk associated with use of the HFD100 Head Fixation Device and will be completing corrective…APO-TRAVOPROST-TIMOP PQ: missing the documented justification for the results obtained.
The affected lot is missing the documented justification for the results obtained.Aesculap Inc. Surgical Instrument Sets
AIC has become aware of the sales and distribution of certain medical devices into the Canadian market without a medical device license from Health Canada.Raz-AT, Raz-CAT, Raz-AP, Raz-SP (Mobile Shower Commode Chairs)
Raz decided a safety enhancement action that we are implementing for the Front and Rear Open (FAR) seats.UniCel DxI 600 and 800 Access Immunoassay Systems
Beckman Coulter UniCel DxI 600 and 800 instruments fail to start after rebooting because the AuObj.exe software does not launch.Firstar® CPR Face Shield
Identified as unauthorized/misreppresented/counterfeit by the manufacturer.
Wyld Canna Inc d.b.a Wyld Canna recalls Real Fruit Mixed Berry CBD Gummies due to packaging and labelling issue
The affected products are packaged in the wrong pack.Important Safety Information on Yescarta (axicabtagene ciloleucel) and the Risk of Cerebral Edema in Primary Mediastinal B Cell Lymphoma (PMBCL)
Patients being treated with Yescarta for primary mediastinal B-cell lymphoma (PMBCL) may be at increased risk for developing cerebral edema, including fatal events…Beckman Coulter AU Immunochemistry System- HDL/LDL Cholesterol Assay
LDL cholesterol OSR6x96 does not meet the triglyceride interference claim per the BAOSR6x96 v10 IFU which states "no significant interference up to 1,500 mg/dl…Vanta/Sequentia Lt Clinician Programmer Application
The Vanta A71200 CP app V2.0.2465 and V2.0.2683 will display a "system error" if the user selects the start usage button twice when interrogating a new implantable…Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.Tempus Pro
The user/operator manual references the term 'invasive pressure', which includes intracranial pressure (ICP) and bladder pressure (BDR) as selectable channel labels.Carestation 600 and 700 Series Anesthesia Systems
Unexpected shutdown of Carestation 600 and 700 series anesthesia systems containing certain power management boards when AC mains power is disconnected or AC mains…
JC Green Cannabis Inc. recalls certain Jonny Chronic dried cannabis products due to labelling issue
The labels for the affected products have incorrect cannabinoid values.A little guidance
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