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Displaying 1 - 15 of 4509 items.
Olympus found that certain lots of the CV-190 do not start up properly and as a result, the image from the endoscope is not displayed when the operations listed below are performed because parts that deviated from the specification were assembled into…
RecallHealth product recall | 2023-09-22
Zimmer Biomet Canada is initiating a lot specific recall for the Zimmer dermatome blades (00-8800-000-10) in Canada. There have been 38 complaints received related to skin grafts being thin and non-uniform when using the affected blades. The issue would…
RecallHealth product recall | 2023-09-21
Affected lot may contain the presence of glass particulate.
RecallHealth product recall | 2023-09-20
In normal use, the laser is activated when the user sets the device to the "armed" state and when the foot pedal is depressed in the "armed" state. (the laser is deactivated when it is not in the armed state). However, there were reported events where…
RecallHealth product recall | 2023-09-20
Lundbeck Canada Inc. has informed Health Canada that two lots of Sabril (vigabatrin) 500 mg powder for oral solution, in sachet format, were found to contain trace amounts of another prescription drug, tiapride.
Sabril is a prescription drug used…
AlertPublic advisory | 2023-09-19
Affected lot may be OOS for related compound CZ RC1
RecallHealth product recall | 2023-09-19
GE Healthcare has become aware of an issue where images from two different patients may be contained in a single study when stored in Centricity Enterprise Archive (EA) and/or Enterprise Archive (EA). This issue could contribute to an adverse patient…
RecallHealth product recall | 2023-09-19
Health Canada is warning consumers about unauthorized health products it seized from a Tokyo Beauty and Healthcare store in Richmond, B.C. (120 - 8191 Westminster Highway). The products are labelled to contain prescription, controlled or over-the-counter…
AlertPublic advisory | 2023-09-18
On 05/05/2023 customer in lab in Switzerland identified that two Multichem® S Plus vials were cracked at the bottom and material was leaking from the vial. No actual end-user/patient harm was identified as a result of the cracked vial.
Recall start…
RecallHealth product recall | 2023-09-18
It has been determined that transferrin ref OSR6152 lot 2573 does not meet the reagent stability claim stated in the Instructions For Use (IFU). Customers may experience reagent blank shifts, calibration failures, and/or QC failures.
Recall start date…
RecallHealth product recall | 2023-09-18
The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material.
Recall start date: September 1, 2023
RecallHealth product recall | 2023-09-18
There was a gas filter used in a fluid bearing line of the custom tubing pack. All computed tomography perfusion (CTPs) that were manufactured before the introduction of the new filter type and have not yet expired are affected. Preventive measure: a new…
RecallHealth product recall | 2023-09-15
Abott is informing customers of a rare potential for a bluetooth circuit component issue on subset of Neturino Implantable Cardioverter Defrbrillators (ICDs) and Cardiac Resynchronization Therapy Defribrilators (CRT-Ds) manufactured prior to April 2022.…
RecallHealth product recall | 2023-09-15
Reports of system error during preoperative calibration self-tests of the Hugo robotic arm cart assembly. After recalibration attempt, the robotic arm cart assembly will be prevented from entering teleoperation even if the calibration is successful. This…
RecallHealth product recall | 2023-09-15
Health Canada is advising about unauthorized health products for lightening skin or treating skin conditions (such as eczema or psoriasis) that may pose serious health risks. The products are labelled to contain or have been tested and found to…
AlertPublic advisory | 2023-09-13