Search

Cordis is recalling specific lots of ANGIOGUARD™ RX / XP Emboli Capture Guidewire System, Cordis has identified that there is a potential for separation of the ANGIOGUARD™ RX / XP delivery system and capture sheath. The potential impacts of separation…

Steris identified through customer complaints that the LB53 light handle covers may separate from the light handle (detach and fall off) during use. Through additional investigation Steris has determined the issue to be associated with the specific lots…

During a ventilation sequence, the user started the "100% O2" function. This function lasts for two minutes but can be interrupted by pressing the 100% O2 key. Note: after the 100% O2 function has been used, the FiO2 setpoint originally entered is…

Two potential Hamilton-C6 Ventilator malfunctions detected following an inspection by Hamilton Medical Ag.:  Malfunction 1: Safety ventilation can be triggered by switching to an adaptive mode. Malfunction 2: The display can be restarted by…

Some lot numbers of collection tubes Vacuette * K2 EDTA have experienced an issue of clotting. This was caused by insufficient amounts of EDTA additive sprayed in the tubes. Recall start date: March 7, 2023

Hole in the adaptor strap may be larger than the river head mounted to hold the trap in place.  Strap could detaches from the portable scale adaptor during a patient transfer with the lifting equipment. It could lead to their fall, potentially…

During our global market surveillance activities, we have become aware of cases in which the software on the Infinity® Central Station drops peaks on narrow waveforms causing the Infinity® M300 to fail the requirements of the standard IEC 60601-2-27.…

This notice concerns issues with DICOM export from the virtual simulation module and issues with import of virtual simulation plans in Raystation, Rayplan 10a, 10b & 11b a including service packs. Recall start date: February 17, 2023

Medtronic was made aware of a supplier calibration issue during the contract sterilization process that may lead to unsterile product. Recall start date: March 1, 2023

Olympus has received complaints that the clip did not come out of the tube sheath during the procedure. investigation by Olympus confirmed the tube sheath is longer than specifications which prevents the clip from being extended. Absence of treatment,…

Maquet Cardiopulmonary GmbH determined two trends for complaints regarding the Heater Cooler Unit HCU 40: degraded internal drain hoses and leaking vacuum valves. This recall will inform users, and give instructions to replace affected parts during next…

Thermo scientific™ Hp StaR™ lateral flow kits are failing to meet IFU criteria with multiple strip giving false positive results with known negative samples and also false positive result on substrate diluent. Recall start date: March 10, 2023

While conducting safety disk testing, expired tubing was used on the test fixture equipment between April 01, 2022 and July 31, 2022. when using the obsoleted, and expired catheter extender tube, 0004-00-0033-01 during the static inflate/deflate test…

Radiometer has become aware that there is a problem relating to the Aqure System (stand alone software system) used in combination with the third party device Lumiradx that may result in patient mix-up. Currently there are no customers in Canada using…

During investigational testing of the Habib™ Catheter with the ERBE VIO 3 generator (compatible 3rd party device), an issue with the generator setting in the Habib™ IFU (50738103) was identified. From the results of this testing, it was…