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Olympus is taking this recall action after discovering that the Thunderbeat's blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position. Olympus is requesting healthcare facilities…

When using this product, the footrest can loosen and fall off in some circumstances, which may result in a foot injury to user. Recall Start Date: September 15, 2023

Ortho Clinical Diagnostics (Quidelortho) determined that lots 5905-3348-1557 and 5905-3348-2899 of Vitros Lipase Slides include carts which may contain consecutive slides that may not function as intended. Quidelortho estimates that approximately 1.4% of…

Complaint trending revealed an adverse trend of complaints stating that a LMS surgical operating microscope unexpectedly shut down caused by a defective 24VDC power supply which is used inside the surgical operating microscopes Provido, Proveo 8 and M530…

Failure description: several complaints were received where the plug (the one at the opposite side of the tubing) became detached from the In2Flow nasal cannula, causing leakage due to unintentional disconnection of that part. This may result in degraded…

In the course of post market surveillance activities and our internal quality checks, we identified that the sterile packaging barrier might be damaged for certain batches. Recall Start Date: August 7, 2023

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…

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…

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…

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…

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…

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…

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

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…

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.…