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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…

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…

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…

The pedal body may detach from the pedal spindle and/or the pedal spindle may break, posing a fall hazard. As of November 28, 2023, the company has received 1 report of the pedal body detaching from the spindle in Canada, and no report of injuries. In…

The affected product is being recalled from the marketplace due to possible Salmonella contamination.

Philips has been informed of an event in which the structural integrity of the Panorama 1.0T HFO system components failed due to unintended excessive pressure buildup of helium gas during a magnet quench. During a quench, a large amount of helium…

The affected products are being recalled from the marketplace due to possible Salmonella contamination.

Product sold without market authorization (DIN) Canada. Product contains undeclared pancreatin that is listed on the Prescription Drug List (provides more than 20 000 USP units of lipase activity/dose).

Issue: On certain vehicles, the variable camshaft timing (VANOS) adjustment unit housing bolts could loosen or break. As a result, the camshaft could become incorrectly adjusted and cause the engine to enter a reduced power mode (limp mode) or to stall…

Issue: On certain school buses, the restraining barrier between the entrance door and the first seat may not meet the energy absorption requirements of Canadian regulations. Safety Risk: A barrier that doesn't properly absorb energy could…

BD continues to receive complaints for the product regarding mismatch between the coaxial and the needle in mission kit devices.  Based on the event reported, the internal diameter of the coaxial cannula may be smaller or larger than the external…