Search
Type
Audience
Category
Issue
Last updated
Recall class
Please note: using the search filters may not provide accurate search results for records prior to November 2021. When searching for older records, please ensure that you use the include archive checkbox.
Displaying 1 - 15 of 402 items.
Teleflex Endotracheal Tubes
Teleflex has initiated a voluntary recall due to reports of disconnection of the 15mm connector from the endotracheal tube (et tube) for the affected products.
Recall start date: May 26, 2023
RecallHealth product recall | 2023-06-07
Enzyme Solution Papain Ortho Sera
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…
RecallHealth product recall | 2023-06-02
Endometrin effervescent vaginal tablets; Burkholderia contamination
Affected lot(s) may contain the presence of Burkholderia contamination.
RecallHealth product recall | 2023-06-02
Allen Advance Chest Support With Pad
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…
RecallHealth product recall | 2023-06-01
Ogival Interbody Cage, PEEK
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
RecallHealth product recall | 2023-06-01
Nature's Bounty Kids Multivitamin Gummies; Labelling issue
Affected lots are incorrectly labelled for use in the subpopulation that is less than 4 years of age.
RecallHealth product recall | 2023-06-01
Dextrose 50 mg/mL Injection; Out of Specification
The dextrose content is out of specification in the affected lot.
RecallHealth product recall | 2023-05-31
PhiLaser Type 2.0
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…
RecallHealth product recall | 2023-05-31
Luobuma Jiangya Tablet; Heavy Metal - Arsenic
Affected lot may contain heavy metal (arsenic) above the acceptable limit.
RecallHealth product recall | 2023-05-31
PMS-Pazopanib 200 mg tablet; Presence of Sorafenib
Presence of Sorafenib in affected lots.
RecallHealth product recall | 2023-05-31
G Fuel brand Energy Drinks recalled due to high levels of caffeine
G Fuel brand Energy Drinks recalled due to high levels of caffeine.
The recalled products have been sold nationally and online.
RecallNotification | 2023-05-30
Feather Dream Mint CBD Rapid Spray; No Market Authorization
Product sold without market authorization (DIN) in Canada.
RecallHealth product recall | 2023-05-30
Kootenay Meadows brand Nostrala Firm Surface-Ripened Organic Cheese recalled due to Staphylococcus aureus and generic E. coli
Kootenay Meadows brand Nostrala Firm Surface-Ripened Organic Cheese recalled due to Staphylococcus aureus and generic E. coli.
The recalled product has been sold in British Columbia and Alberta.
RecallNotification | 2023-05-27
Pushtracker E2 & E3 Utilized With Smartdrive MX2+ Power Assist Device
Through design and development work, Max Mobility has identified a software issue with the application. When multiple processes are running on the watch's central processing unit, the application may crash unexpectedly. If this happens, the motor on the…
RecallHealth product recall | 2023-05-19
Uruthira brand Plain Chilli Powder recalled due to Bacillus cereus
Uruthira brand Plain Chilli Powder recalled due to Bacillus cereus.
The recalled products have been sold in British Columbia, Ontario and Quebec.
RecallNotification | 2023-05-19