Medical devicemaker recalls patient lift after 2 deaths reported

Hillrom, a medical devicemaker based in Chicago, has recalled its patient overhead lift device after multiple reports of serious injuries and two patient deaths. 

Advertisement

Hillrom is recalling its Liko Multirall 200 Overhead Lift, used to move patients from room to room in hospitals, rehabilitation facilities and nursing homes, due to customer reports that the strap doesn’t attach to the hook properly. If the strap doesn’t attach, the motor or patient may fall, which could cause serious injury or death. 

The company has received 34 complaints about the device, 22 reports of serious injuries and two reports of patient deaths. 

The FDA said Feb. 22 that it has classified the recall as class 1, the most serious type. 

Read the FDA’s full news release here

More articles on supply chain:
US to send 25M masks to community health centers, food banks in March
Last-minute FEMA waiver let US company export 5M masks monthly despite domestic shortage, probe finds
Biden signs executive order to strengthen US supply chains

Advertisement

Next Up in Supply Chain

Advertisement

Comments are closed.