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During extended operation of the MX40 with the PIC iX, the DHCP (dynamic host configuration protocol) lease can expire on the MX40. If the DHCP lease expires while the device is offline, upon reconnecting with the pic ix, a new IP address will be…

Medtronic has identified a rare potential for reduced or no-energy output during high voltage therapy in Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) manufactured with a specific (glassed)…

During an update of data used in a library shipped with Exoplan or made available on the download portal of Exocad, it was found that the use of a specific combination of an implant, sleeve and drill in a surgical kit can result in a hole being drilled…

Some of the tubes have no gel. Recall start date: May 12, 2023

TheraHoney wound gel is being recalled after a sterility dose audit failure by the manufacturer. Certain lot numbers are affected. usage of non-sterile gel on open wounds or compromised skin could increase infection risk. Recall start date: May 16,…

Olympus has become aware of increased complaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, potentially causing harms to patients.…

The ceiling tube support for the above device consists of an x-ray tube support pull-up section and an x-ray tube support section to which an x-ray tube assembly is mounted, and the tube holding section is secured to the column of the x-ray tube support…

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…

The Vitros Chemistry Products Calibrator Kit 20 is used to calibrate Microtip assays C3, C4, IgM, IgA, IgG, and transferrin. Vitros Calibrator Kit 20 contains five calibrator levels. Although lot 2022 met all initial release criteria, vial to vial…

It has been found that the c-arm and table may not be able to operate because the soldering on the tableside console printed wiring board was not done properly. Recall start date: May 8, 2023

During the transportation of the product (only one box) from McKesson Canada to the customer, the vehicle was involved in an accident thereby exposing the products to external freezing weather conditions as low as -16°c for approximately 2 days. Due to a…

As a follow up to the section 64 report sent on April 3, 2023, it has come to our attention that while the upgrade to version 19.4 software has been successful in the vast majority of cases, we have identified an issue when upgrading some units. The…

During the course of global market surveillance activities, the manufaturer has become aware of cases in which the resuscitaire infant radiant warmer with the optional scale could display inaccurate weight values. There is a potential for the mattress…

Stryker has determined that the affected pad-paks may be rendered inoperable due to depleted battery cells. As a result, the affected pad-paks could potentially fail to power on the device if needed for use. Recall start date: May 3, 2023

Recall being conducted as the device does not have a medical device licence in Canada and due to design flaw. Recall start date: March 27, 2023