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Baxter Corporation is issuing an urgent medical device recall for the Amia Automated Peritoneal Dialysis (APD) cycler set listed due to an increase in complaints related to failure alarms for wet cassette integrity test occurring on the Amia devices.…

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

Abbott recently observed an increase of reports (complaints) in which the power connector plug became frayed or damaged over time. Damage and fraying of the power connector plug can occur with repeated bending or manipulation beyond 90 degrees. Fraying…

There is an issue where HL7 messages from Change Healthcare Radiology Solutions (CHRS) may not update records in Change Healthcare Image Repository (CHIR) and Change Healthcare Workflow Intelligence (CHWI). Recall start date: September 7, 2023

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

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

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

Siemens Healthcare will be informing customers about potential dot- or line-shaped artifacts caused by the presence of lubricating grease within the headband of the over-ear headphones listed below when used during head examinations with the Magnetom MRI…

Arjo has observed an increasing complaint trend on the following failure modes occurring on Arjo medical beds assembled with the Indigo modules: unanticipated device self-acceleration while being operated by a caregiver, unexpected movement without any…

Stryker has discovered the potential for the Triathlon Fixation Peg to be missing the hex hole feature preventing the peg from assembling with the slip torque handle. Recall start date: August 21, 2023

These unauthorized nitrile medical examination gloves were distributed by Frontier Dental Supply Inc. between March 15, 2022 to December 24, 2022. These products, which were intended to European market, entered Canada without authorization from Health…

The calibration of the force sensor used to detect occlusions may shift over time. If the force sensor calibration shift is large enough, the pump will display a system failure alarm (including force sensor BGND test, force sensor bridge test, or force…

The following malfunctions and nonconformances were observed during Trexo lab-testing and Trexo design reviews of the device, Resulting in this voluntary device recall and proposed field correction. Electromagnetic (EM) radiation levels above threshold (…