Search

The juicers can rupture during use, striking consumers and posing a laceration hazard, or can leave small particle shavings in the juice, posing an ingestion hazard to consumers. As of May 29, 2023, the company has received 1 reported incident in…

The rear switch trigger can fail to rebound after being pressed, which can cause the unit to activate unexpectedly, posing a potential laceration hazard. As of May 10, 2023, the company has received 3 reports of incidents in Canada, and 1 report…

Nestlé Health Science is recalling twelve lots of Nature’s Bounty Kids Multivitamin Gummies (NPN 80117143) because the product’s label does not indicate that the gummies should not be given to children under four years of age. Giving these products to…

Affected lots are incorrectly labelled for use in the subpopulation that is less than 4 years of age.

Biomerieux identified a manufacturing event that may contribute to elevated rates of false negative results while using the Biofire RP2.1 panel. Biomerieux has not received any false negative complaints from the field but, out of an abundance of caution…

Baxter Corporation is issuing an urgent medical device recall for the Allen Advance Chest Support to inform customers of the potential for the device to crack where the chest base and prone supports attach to the carbon fiber operating room (or) table…

Stryker has determined that size 11 (11mm) height peek Ogival Interbody Cage (OIC) was incorrectly laser marked as having a size 10 (10mm) height. Recall start date: May 19, 2023

Affected lot may contain heavy metal (arsenic) above the acceptable limit.

During the course of global market surveillance activities, the manufacturer has become aware of cases where Oxylog 3000 Plus emergency and transport ventilators have stopped ventilation due to empty batteries despite being reconnected to the mains power…

Currently, the Hemospray instructions for use states "Potential complications: when spraying in the retroflexed position, Hemospray powder may adhere to the outside of the endoscope. This may result in difficulty repositioning / removing the endoscope,…

The dextrose content is out of specification in the affected lot.

A concern with the software network binding of the Universal Copy  Service (UCS), an ILMN proprietary software component present on ILMN instruments. The concern expressed was that the software process running as a tcp service was found to bind to…

Presence of Sorafenib in affected lots.

Health Canada advised that the Philaser Type 2.0 device is considered a class III medical device and requires a licence.  The Philaser Type 2.0 device is not currently licensed, so we have stopped sales and advertisement of the Philaser Type 2.0…

Issue: On certain RV trailers, the exhaust exit for the water heater was installed too close to a slide-out room. As a result, exhaust fumes and carbon monoxide from the water heater could enter the trailer. Safety Risk: A buildup of exhaust…