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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…

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

The instructions for use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient line connections with single collection chamber chest drains. Recall…

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…

Venue Go standard carts may have an internal failure of the vertical/horizontal tilt adjustment mechanism. Recall Start Date: September 19, 2023

Presence of particles in the affected lot.

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…