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 18 minutes ago
CanadaNitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
The affected products are sold for inhalation without market authorization (DIN) in Canada.Revolution Ascend
Potential security vulnerability impacting AW server deployed via Edison Health Link (EHL) based CT smart subscription on certain Revolution series CT systems.Mixing Bowl And Spatula, 20- Pack
Zimmer Biomet is conducting a lot specific medical device recall removal for the mixing bowl and spatula.Dexcom G7 iOS CGM App
G7 iOS app display flickers sequentially through previous Estimated Glucose Values (EGVs) and before displaying the current EGV.Apo-Fluoxetine: The impurities are out of specification and out of trend
The impurities are out of specification and out of trend in the affected lot.
TJ Trading Co. Inc. products recalled due to missing mandatory hazard labelling
These products do not meet the Cosmetic Regulations in Canada.Stryker InZone® Detachment System
Stryker Neurovascular has identified an issue affecting certain lots of InZone® Detachment System devices.Cardinal Health™ Angiography Pack and Catheterization Packs
Cardinal Health™ was recently informed of a medical device recall from Medline Industries concerning the Convenience Kits referenced.Medline ENFit G-Tube Connector
Medline ENFit G-Tube Connector (ENFIT1010GC) is recalled.
Think twice before injecting peptides bought online: unauthorized products can seriously harm you
Health Canada is warning consumers about the serious health risks of using unauthorized injectable peptide drugs.Medline Neuro Sponges
Specific item(s) and lot(s) of Medline neuro sponges are recalled due to a potential out-of-specification for endotoxin.Nucletron B.V. Intrauterine Tube
Elekta are informing customers of a safety concern regarding the detachment of the tip of the Intrauterine Tube (IU tube) with a 4mm diameter that remained within a…ACE Surgical Supply® PGA (Polyglycolic Acid) Absorbable Sutures & Absorbable Gut Sutures
BioHorizons Canada is performing a recall for products manufactured by ACE Surgical.Aved products recall: No market authorization
Products sold without market authorization (DIN) in Canada due to third-party branding.Olympus Connecting Tubes
Olympus identified through complaint review that version 2 connecting tubes may fail prematurely, with lock levers detaching or breaking earlier than expected.AneurysmFlow
Philips has determined that the mafa ratio does not provide reliable prognostic information regarding aneurysm occlusion following flow diverter stent treatment.Edwards EVOQUE Tricuspid Delivery System
Edwards Lifesciences is notifying customers of a voluntary recall (correction) involving a labeling update for the Edwards EVOQUE Tricuspid Valve Replacement System.Dimension® Creatinine (CRE2)
Siemens Healthineers has confirmed, through investigation of customer complaints, a potential for imprecision in Dimension® Creatinine (CRE2) quality control (QC) and…Medline Convenience Kits containing Namic RA Syringes
Kits containing Namic Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA Syringes) have been recalled by Medline due to a potential risk of the syringe…Health First Vitamin E capsule; Undeclared active ingredient
Affected lots contain undeclared active ingredient.Kiwi® Vacuum Assisted Delivery System
The device may break at the Traction Force Indicator (TFI) joint during use when traction is applied at approximately a 45-degree angle.DermaHealer UVB Light Therapy Lamps
DermaHealer UVB light therapy devices were distributed to customers in Canada without a Canadian Medical Device Licence (MDL) as required under the Medical Devices…Flamingo Funnel™
Packaging defect: A non-gamma-compatible drape degraded under heat, causing pinholes and possible loss of sterility.A little guidance
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