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Software versions prior to 2.04 show a waveform while in suspend processing, while software version 2.04 and above do not show a waveform. Both software versions show an error message stating "ECG processing suspended" in the waveform zone, "?" in the…

Affected lot(s) may contain the presence of Burkholderia contamination. 

Baxter Corporation is issuing an urgent medical device correction for the Voalte Patient Safety, previously branded as Navicare Patient Safety, software versions 3.9.200 through 4.0.401. Baxter identified a potential risk where the "safety" monitoring…

Philips has become aware of a software login issue associated with specific models of Mobilediagnost wDR systems running on Windows 10 operating system preventing use of the system. This issue occurred because the software certificate protecting the…

Ortho™ Sera Papain is used to enhance reactivity of Ortho™ Sera red blood cell antigen typing reagents and red blood cells when used in in-vitro immunohematology assays. Through a customer complaint investigation, the reactivity of Ortho™ Sera Papain of…

The affected product is being recalled from the marketplace due to possible Listeria monocytogenes contamination. The recalled product has been sold in Ontario.

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

Issue: On certain travel trailers, the spare tire carrier could break and separate from the trailer. Safety Risk: A spare tire carrier that falls from the trailer could become a hazard for other road users and bystanders. This could create a…

Issue: On certain fire trucks,the pump shift solenoid may become corroded and fail. If this happens, power to the pump control module may be lost, and the vehicle may not shift into pump mode. Safety Risk: A loss of power to the pump control…