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The axis camera ceiling tile is not fitting properly in some domestic institution ceiling tile grids that have a thinner style grid frame. In these cases, modifications to the site's suspension grid or the natus ceiling tile might be required to provide…

Under certain sporadic circumstances the Sensis Vibe Hemo System with VD12A software the Co (cardiac output) measurement using the thermodilution method will temporarily no longer be possible. This happens without any obvious reason. When the issue…

When patient demographic information is entered into the system and the patient information is saved or exported to a folder, in very rare situations, the demographic information that is displayed is that of the previous patient instead of the current…

This update is specifically targeted to improve the robustness of the sequoia caster-assembly. The front casters cannot fall of the Sequoia system, since the wheel locking/swivel control rod runs through the caster shaft. If the bolt comes out, the…

A software defect was discovered, whereby in certain circumstances, a change to a reference range value that was canceled by the operator could nevertheless be saved, which may lead to incorrect reference range being set on the device. The software…

Siemens Healthcare is notifying customer of a potential failure in the clip store function on the Acuson Juniper ultrasound system. In Juniper 1.0 the clip store function does not work when the ultrasound system has a disk full error. The purpose of this…

Reports received of a small hole or damage in the area of the maple leaf symbol in the corner of the healthy apparel disposable masks. Recall start date: Jan 24, 2022

There is the potential for the metal tip on the Da Vinci Xi And X 12-8 Mm Cannula Reducer (PN 470381-11) to get dislodged from the cannula reducer plastic shaft. Recall start date: Dec 20, 2021

Baxter Corporation is issuing an urgent medical device correction for the Minicap Extended Life Pd Transfer Sets. The following products may cause damage if they come into direct contact with the transfer set: Cleaning products such as hand sanitizer and…

Zimmer Biomet is conducting a medical device recall for one lot of the Navitracker Kit A : Knee product, which is a nonpatient contacting device used during computer and robotic assisted surgeries. The product in scope was released for distribution…

The Curad Hot/Cold gel pack with wrap currently has the labeling states "does not contain natural rubber latex". However, the fabric around the gel pack does contain some natural rubber latex. The fabric wrap contains 20% latex thread. There is a risk of…

Potential violation of the rules and regulations related to market approval of some features of the software medical device Cara based on artificial intelligence. Recall start date: Jan 11, 2022

Medtronic has identified eighteen reports where during the advanced evaluation trial period, the percutaneous extension connector has migrated from the future stimulator pocket site along the tunneling pathway. This resulted in difficulty locating the…

GE healthcare (GEHC) MR systems could potentially have a cryogen ventilation system that does not meet the venting requirements. Failure to have proper venting could present a safety issue if the cryogen gas is vented into the MR room during a magnet…

GE Healthcare (GEHC) MR systems could potentially have a cryogen ventilation system that does not meet the venting requirements. Failure to have proper venting could present a safety issue if the cryogen gas is vented into the MR room during a magnet…