WASHINGTON, DC - A news report posted on medtechdive.com states that the U.S. Food and Drug Administration has classified the recent Hillrom's overhead patient lift recall as a Class I recall after the device caused two patient deaths. So far, there have been about 34 complaints filed against the patient lift product, including 22 … [Read more...] about Hillrom Liko Multirall 200 Overhead Patient Lift Recalled Following to Patient Deaths