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Displaying 1 - 15 of 3726 items.

Health alert or recall JAMP-SENNA: Out of Specification
The total yeast and mold count is out of specification for the affected lots. 
RecallHealth product recall | 2022-05-19
Health alert or recall PMS-Montelukast: impurity
Presence of an unspecified impurity near the acceptable concentration limit in the affected lot.
RecallHealth product recall | 2022-05-19
Health alert or recall Shortage of infant formulas for babies with food allergies: what you should know and do
The closure of a large infant formula manufacturing plant by Abbott Laboratories in the United States (manufacturer of Similac®Alimentum)®, has resulted in a global shortage of infant formula. Canada is experiencing a shortage of infant formulas designed…
AlertPublic advisory | 2022-05-19
Health alert or recall Centricity Radiology, Zero Footprint and Pacs Systems
GE Healthcare has become aware of two potential issues where inaccurate distance and area measurements can be displayed. Recall start date: May 5, 2022
RecallHealth product recall | 2022-05-16
Health alert or recall Carescape Central Station
The Carescape Central Station (CSCS) V2 can shut down due to a potential power supply component failure. This can lead to loss of patient monitoring at the central station. Patient monitoring at the bedside is not affected. Recall start date: May 10,…
RecallHealth product recall | 2022-05-16
Health alert or recall Argyle Safety Fistula Cannula With Anti-Reflux Valve
Potential for blood leak to occur with the anti-reflux valve upon treatment completion. Recall start date: May 5, 2022.
RecallHealth product recall | 2022-05-16
Health alert or recall Ks White Nitrile Medical Examination Gloves
After initiating testing by a third-party lab, it was discovered that the tested lots did not meet the astm d6319 standard for medical gloves. Initial testing was received on March 4, 2022 and communicated to the original manufacturer. Confirmatory third…
RecallHealth product recall | 2022-05-16
Health alert or recall Belotero Lidocaine
The recall activities are being conducted due to several temperature excursions on inbound shipment to Canada.  According, to the assessment by the manufacturer, Anteis S.A, no data is available for Belotero products after repeated freezing and…
RecallHealth product recall | 2022-05-16
Health alert or recall SOCLEAN 2 AUTOMATED SUPPLEMENTAL PAP MAINTENANCE DEVICE
Labelling changes were issued for the Soclean 2 such as 1) running the Soclean 2 for a 12-minute cycle time duration obtains a 99.9% reduction of microorganisms, 2) Soclean 2 is not an automated pap disinfecting system but rather an automated…
RecallHealth product recall | 2022-05-16
Health alert or recall Alinity Hs/Hq System
The purpose of this notification is to inform you of a product recall for Alinty Hq analyzer and Alinity Hs slide maker stainer module.  Abbott hematology identified that product information letter (pi-l) 1035-2020 issued for fa18jun2020, which…
RecallHealth product recall | 2022-05-16
Health alert or recall Leucovorin Calcium Injection: Out of Specification
The assay is out of specification in the affected lot(s).
RecallHealth product recall | 2022-05-13
Health alert or recall Health Canada reminds Canadians that plasma pens are unauthorized and may pose health risks, following complaints involving Calgary and North York spas
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
Health alert or recall Plasma pens are not authorized in Canada and may pose health risks
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
Health alert or recall Nim™ Standard Reinforced Emg Endotracheal Tube & Nim Contact™ Reinforced Emg Endotracheal Tube
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
Health alert or recall Breathing System Filter Safestar 55
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
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