The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.
Reason for recall: The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop. Distribution: Worldwide Quantity: 9839 units Lot/code info: All LikoScale Adapter Kits manufactured between 8/27/2013 to 2/27/2025
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.