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Displaying 1 - 15 of 1621 items.
Some of the recalled products may have microbial contamination. Individuals with weakened immune systems, who suffer from a serious pre-existing condition, are at an increased risk of infection if they use the contaminated product.
As of…
RecallConsumer product recall | 2022-05-13
The assay is out of specification in the affected lot(s).
RecallHealth product recall | 2022-05-13
Tree Brewing Co. is recalling the affected products from the marketplace because they contain sulphites which are not declared on the label.
The recalled products have been sold in Alberta and British Columbia.
RecallFood recall warning | 2022-05-13
Health Canada is warning Canadians of the serious danger posed by DigitDots magnet sets that were sold to Canadians online by HD Premier.
These sets contain small, powerful magnets that can be easily swallowed by children of all ages, posing serious…
AlertPublic advisory | 2022-05-12
August 25, 2019
For immediate release
OTTAWA – Health Canada is reminding Canadians that plasma pens are not authorized for sale in Canada and that these devices may pose health risks. Health Canada is also underlining that consumers should be wary…
AlertInformation update | 2022-05-11
November 26, 2018
For immediate release
OTTAWA – Health Canada is advising consumers that plasma pens (also known as “fibroblast” devices) promoted for cosmetic skin treatments such as eyelid lifts, wrinkle reduction and…
AlertInformation update | 2022-05-11
Manufacturer has received reports of events related to airway obstruction while using the impacted device. Not following the instructions for use (IFU) and over-inflating the cuff increases intra-cuff pressure, which can cause the silicone cuff to extend…
RecallHealth product recall | 2022-05-10
Dräger has become aware of one case in which an obstructed Breathing System Filter Safestar 55 was used on a patient during anesthesia. The patient reportedly became hypoxic and had to be reanimated. If an obstructed filter is used on a patient,…
RecallHealth product recall | 2022-05-10
During global post market surveillance activities cases have been reported that the sampling pump 6873493 shows a changing characteristic with increasing operating time, which can lead to the deactivation of the gas measurement during operation. The…
RecallHealth product recall | 2022-05-10
Since Nov. 2020, Arjo has become aware of 2 customer complaints involving overheating of metal part of the device located underneath its frame. The part involved is referred to as the e-bay box. No adverse health consequences (including temporary or…
RecallHealth product recall | 2022-05-10
During continuous post market surveillance, Draeger gathered information and market feedback indicating that there is a need to provide additional information in the instructions for use regarding the potential of the user to incorrectly position the…
RecallHealth product recall | 2022-05-10
The complaint bottle contains Naphazolin HCl 0.013% and Glycern 0.26%.
RecallHealth product recall | 2022-05-09
Karl Ttorz Endoscopy Canada is conducting a field action for specific serial numbers of C-View endoscopes with the potential to lose image when monopolar electrocautery is activated.
Recall start date: May 2, 2022
RecallHealth product recall | 2022-05-09
The STO2 values may be inaccurately low when using either the fore-sight elite tissue oximeter module (Model HEMFSM10) or the fore-sight elite absolute tissue oximeter monitor (Model 01-06-3000) with the fore-sight elite large sensor (…
RecallHealth product recall | 2022-05-09
Carescape R860 ventilators, and Engström Carestation and Engström Pro ventilators with affected field replacement batteries - insufficient battery backup power resulting in premature shutdown of the ventilator when not connected to AC mains power supply…
RecallHealth product recall | 2022-05-09