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
Dual Mobility Vivacit-E® Vitamin E Bearing
Zimmer Biomet is conducting a medical device recall for one (1) lot of the Dual Mobility Vivacit-E® bearing due to a commingle.Catalyft™ PL Expandable Interbody System, Interbody Cage
This notification is to inform customers of the potential for loss of lordosis and ensure that they are aware of updates that Medtronic is making to the surgical…Culture Kizos inc./Kizos Culture inc. recalls Coterie Double-Infused Fruity Pebbles Blunt due to microbial contamination
The affected products may contain mould.Atlantiscan: Broken Vials
The vial is broken in affected lot.ITOVEBI (inavolisib) and the Risk of Life-Threatening Ketoacidosis
Two cases of life-threatening or fatal ketoacidosis have been reported in diabetic patients treated with ITOVEBI in the post-market setting.LOGIQ P10
GE Healthcare has become aware of an issue on certain LOGIQ P9 and LOGIQ P10 series ultrasound systems with system software version R4.5.7.Low Prof Lckng Screw F/Im Nail, Sterile
The affected product lots are being recalled because, although the etched length on the screw is correct, the length marked on the external packaging is incorrect.Magseed Pro Magnetic Marker System
During residual and particulates testing it was discovered that cotton fibers were present on the markers.Lisinopril HCT 20/25mg: Out-of-specification test results
Affected lots were recalled following assay stability out-of-specification test results.Filter Set For Cook K-Mar 5200 Pumps
For the device in question and, therefore, what was imported as a Class I device, has now been determined to be a Class II device.IMRIS Systems
This recall is being initiated to address a notification received by IMRIS Imaging, Inc.Precision1 One-Day Contact Lenses
Alcon is initiating a medical device recall for lot A8041128 of its Precision1™ Daily Soft Contact Lenses.Ziptight, Acute Ac Joint Implant, Single Ziploop
Zimmer Biomet is conducting a medical device recall for one lot of the Ziptight, Acute AC Joint Implant, Single Ziploop.Various Magic BM products recalled due to missing mandatory hazard labelling
These products do not meet the Cosmetic Regulations in Canada.Alinity HQ Analyzer
An issue has been identified in Alinity HQ Analyzer software versions 5.0 to 5.10.1.Carescape™ Central Station
GE healthcare has identified an issue affecting Carescape™ Central Station (CSCS) with software version v3.0.5, which can cause the system to enter a continuous reboot…Endoscopy Trocar
Aesculap AG identified through investigations of complaints that the yellow sealing component of the affected reusable trocar systems 10mm and 12mm exhibits uneven…Importation of US-Authorized Fludarabine Phosphate Injection, USP due to the Current Shortage of Canadian-Authorized Fludarabine Phosphate Injection
There is a shortage of Fludarabine Phosphate Injection in Canada.Sensi Brands Ltd. recalls Wintermint Chillows and Cinnamon Chillows due to product quality issue
The products contained inaccurate THC values that differ from the label.Expanded recall: Various Rocco Donna Professional hair products recalled due to missing mandatory hazard labelling
The recalled products do not meet the Cosmetic Regulations in Canada.Cardinal Health-Presource® Kits Containing Clearlink Components IV Sets
The reason for this recall is to notify users that the specific lot of the anesthesia kit contains Clearlink IV sets manufactured by Baxter Healthcare which have been…AHCC: Incorrect label
Incorrect label (AHCC 500mg 60 capsules NPN 80036494) may be appended to affected lots that contains: Advanced Bone Protection 40mg 30 capsules NPN 80014819.GE HealthCare Nuclear Medicine Systems
GE HealthCare stop use notice for certain nuclear medicine systems that are past the end of guaranteed service (systems that have not been manufactured for many years…A little guidance
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