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Ambu has received information on two incidents where Ambu® aView™ 2 Advance caught fire when mounted on the vesa holder of the aCart™ compact, due to incorrect length screws used penetrating the lithium-ion battery of the device. Investigations have…

Health Canada has determined that the recalled blinds do not meet the Corded Window Coverings Regulations and pose a strangulation hazard. The product can create loops exceeding 44cm. Young children may pull looped cords around their neck…

Olympus is taking this recall action after investigating reported complaints about issues inflating, deflating and/or retrieving the devices, as well as reports of bursting and leaking. Olympus has received reported adverse events involving foreign body…

Baxter Corporation is issuing an urgent medical device recall for the Amia Automated Peritoneal Dialysis (APD) cycler set listed due to an increase in complaints related to failure alarms for wet cassette integrity test occurring on the Amia devices.…

Our recent interference testing has shown that the presence of lubricants in the vaginal specimen may interfere with the prom test result, which deviates from what is presented in the instructions for use. The defectiveness was discovered 2023-11-08.…

The affected products are being recalled from the marketplace due to various non-compliances related to caffeine content and labelling requirements.

The cooktop’s burners can remain on after being turned to the “off” position, posing a burn hazard to consumers. As of December 1, 2023 the company has received no reports of incidents or injuries in Canada.

In June 2023, due to market disruptions outside of our control, Cardinal Health changed the supplier for the cotton used to manufactur Webril™ Undercast Padding. Although the Webril™ Cotton Undercast Padding continues to meet product specifications,…

The impurity free salicylic acid is out of specification in the affected batches.

The quality issue under investigation is applicable to the "connection cable venous probe, l0.23m".  The part causing the nonconformance under investigation is responsible for data transmission between the Cardiohelp-i and the venous probe. A…

Following analyses carried out by Groupe Marcelle Inc., the results showed that the affected products do not meet microbial standards due to traces of mould that develop over time. As of November 23, 2023, the company has received 5 reports of…

Smiths Medical has identified a manufacturing defect affecting specific rotator lots. Within this population, the inner diameter of the device's o-ring may be oversized affecting seal integrity. Recall Start Date: November 9, 2023

Health Canada's sampling and assessment program has determined that this product does not meet the Consumer Chemicals and Containers Regulations, 2001 (CCCR, 2001) in Canada. Specifically, testing showed that the product was "very flammable…

Baxter is issuing an important product information letter to communicate that the cardiovascular surgery marketing brochure (Ref ca-as32-210022 (English) and ca-as32-220004 (French)) that was distributed for the products listed above contains inaccurate…

It has been determined that the terminal block used to secure the power supply cable for the gradient coil of the MRI system was not secured as designed. Because of this, the cable became disconnected, and arcing occurred. Melting of the cable due to…