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 1 minute ago
ARCHITECT "I" System - i2000SR Processing Module - Class 4
An issue has been identified with the 5 Amp (5A) diode used in the Induction Heater (IH) Control Module on the ARCHITECT i2000SR IH Kit (optional hardware).NICO Myriad™ 19x21.5 MHP Paediscope
Stryker identified the Myriad Paediscope handpiece may not fit through the included adapter to connect the handpiece to the neuroendoscope.Cochlear Implant Model CI1012
Cochlear Limited is conducting a recall involving a limited number of specifically identified CI1012 Cochlear Implants.EMIT® 2000 Quinidine Assay
Siemens Healthineers has confirmed through the investigation of customer complaints and internal investigation that the potential for Repeatability precision to be…HemosIL AcuStar HIT-IgG(PF4-H)
A performance issue was identified with HemosIL AcuStar HIT-lgG(PF4-HL ) for the Lot B38062.Flintstones Complete Multivitamins and Minerals: Recalled from wholesalers (Distribution Error)
Customer-returned products were inadvertently reintroduced into saleable inventory and distributed to the wholesale level.cobas® c 303 analytical unit
An issue has been identified where vacuum tubing of the cell rinse unit of the cobas c 303 analytical unit prematurely deteriorated.Claritin Allergy Tablets 10 mg: Recalled from wholesalers (Distribution Error)
Customer-returned products were inadvertently reintroduced into saleable inventory and distributed to the wholesale level.Aleve 200 mg caplets: Recalled from wholesale (Distribution Error)
Customer-returned products were inadvertently reintroduced into saleable inventory and distributed to the wholesale level.CareLink™ SmartSync™ Device Manager
An update within the Apple iPad Operating System (OS) may reduce Bluetooth disconnections between the Medtronic CareLink™ SmartSync™ (SmartSync) device manager software…Tracoe Experc Percut Dilation Tracheostomy Set W/Trachatraumatic Inserter
Tracoe is issuing a Field Safety Notice as the application bears a very low risk that the silicone sleeve may detach from the guiding catheter when removing the…Philips Allura Xper Systems
Philips has identified a software issue that may cause the Flexvision software application to become unresponsive during clinical use.FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version HW 2.3
Under specific conditions following a deep battery discharge, error 29515 may occur during startup of a FreeO2 HW 2.3 device using software package 1.4.2 and prevent…TruSystem 7000 and TruSystem 7500 Surgical Tables
Baxter Corporation is issuing a voluntary correction for certain TruSystem 7000 and TruSystem 7500 surgical tables due to a reported issue with the main lift mechanism.Cardinal Health Presource Kits
Cardinal Health Presource® has identified various kits that may contain a component impacted by the welmed, extension tubing sets component.Avantage Inserter Handles and Grippers
It was identified while using the Avantage inserter handles and grippers during the implantation of the acetabular shell, that the acetabular shell may not consistently…Perma-Sharp Sutures
Perma-sharp sutures are manufactured for Hu-Friedy by 2 manufacturers.Fluoroplastic Vent Tube
Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization.Cardinal Health General Procedure Tray
Cardinal Health was recently informed of a medical device recall from Becton Dickinson concerning the BD Alaris™ Pump Infusion sets used with BD Alaris™ pump module…Embletta MPR PG
Natus has become aware of complaints related to certain Embletta MPR devices where the device is unable to correctly format its internal memory.FreeO2 Automated Oxygen Therapy Device Adult & Pediatric
A battery reading error may occur when certain Freeo2 HW 1.2 devices are restarted following an upgrade from software version 1.2.X to 1.4.X.Medline Bariatric Rollator
Specific lots of Medline BariatricRollator (SKU: MDS86800XWS), are being recalled due to the front fork stem bolt/wheel assembly disconnecting from the rollator frame…Lumify Ultrasound System
Potential issues with the Lumify Diagnostic Ultrasound System which may prevent or delay scanning functionality: Due to a software issue, the Lumify application may not…A little guidance
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