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Specific lots of Cardinal Health Monoject™ luer-lock tip syringes (6 and 35 ml) have demonstrated recognition and compatibility issues with certain syringe infusion pumps. As a result, Cardinal Health recommends that they not be used with syringe…

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…

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

Smart tags (bluetooth powered tracking devices) were placed in multiple loaner devices manufactured by Stryker Endoscopy without undergoing verification and validation testing to ensure no adverse effect on product functionality. Recall start date:…

The tracheal intubation scopes, LF-V and LF-P, have been listed as compatible with Olympus endoscope reprocessors (models OER-pro and OER-elite). the OER-pro endoscope reprocessor was the first Olympus model introduced among this series and was launched…

The 9-inch image intensifier for the impacted systems can become detached if the systems encounter a large impact force when moved.  Recall start date: May 25, 2023

Siemens Healthcare Diagnostics Inc. has confirmed the occurrence of discrepant high glucose results in samples with glucose results on the lower end of the reportable range (at or below 54 mg/dl) when using the above listed lots of BGEM test cards in…

There is the potential that an incorrect type of secondary latch could have been installed on the northeast (ne) and/or northwest (nw) bedside panels for certain Giraffe Omnibed Carestation devices (serial number specific). With the incorrect type of…

BD has received complaints regarding mismatch between the coaxial and the needle in mission kit devices, where the coaxial cannula internal diameter and length exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle…

Medtronic is initiating a voluntary recall for specific production lots of Shiley™ Adult Flexible Tracheostomy Tubes with Taperguard™ Cuff and Cuffless with disposable or reusable inner cannulas. This recall follows reports from customers that the device…

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…

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…

Zimmer Biomet is conducting a medical device correction to update the compatibility matrix as referred to in the instructions for use (IFU) for the CoCr Femoral Head XS. The update is to remove the compatibility with the Epsilon Durasul Constrained …

BD has received complaints regarding mismatch between the coaxial and the needle in mission kit devices, where the external diameter of the biopsy instrument being larger than the internal diameter of the coaxial needle. Recall start date: February 28…