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Displaying 1 - 15 of 3716 items.
The assay is out of specification in the affected lot(s).
RecallHealth product recall | 2022-05-13
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
COMIRNATY received a Notice of Compliance (NOC) under the Food and Drug Regulations on September 16, 2021, replacing the previous authorization under the Interim Order.
On March 15, 2022, COMIRNATY also received a NOC for an additional formulation…
AlertHealth professional risk communication | 2022-05-09
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
Customer complaint on over-inflation (abnormal inflation issue) occurring during the product installation, Preparation to initiate therapy or product use. In none of those events, any injury or health consequences were reported. the products in the…
RecallHealth product recall | 2022-05-09
Reports of products having torn corrugated breathing tube.
- Should a tear be detected before use, a delay may be experienced while another product is located.
- Should a tear be detected during use, this may result in a leak and…
RecallHealth product recall | 2022-05-09