The recall includes 108,816 Medfusion Syringe Pumps that were distributed across the U.S. and Canada, according to an Oct. 6 FDA post. Hospitals use the product to administer fluids and medications.
“A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm,” the FDA said, adding that any device could have this issue but many consumer reports involve pumps made before April 2022.
At the Becker's 11th Annual IT + Revenue Cycle Conference: The Future of AI & Digital Health, taking place September 14–17 in Chicago, healthcare executives and digital leaders from across the country will come together to explore how AI, interoperability, cybersecurity, and revenue cycle innovation are transforming care delivery, strengthening financial performance, and driving the next era of digital health. Apply for complimentary registration now.