The FDA has issued another umbrella-style Emergency Use Authorization, covering infusion pumps, devices and accessories that are in high demand for treating patients with COVID-19. The move is similar ...

A multidisciplinary team was assembled to perform an FMEA of the i.v. medication administration process incorporating pump technology and to report its findings to the hospital performance-improvement ...

Iradimed Corporation announced that it has received FDA 510(k) clearance for its next-generation MRidium® 3870 IV Infusion Pump System, making it the only supplier of non-magnetic MRI-compatible ...

Am J Health Syst Pharm. 2006;63(16):1528-1538. We report anticipated failure modes that occurred postimplementation despite the implementation of our recommended actions. Most of the listed failures ...