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FDA (Device enforcement)Recalled 2025-05-30class i

Baxter Healthcare Corporation: Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScal

Hazard

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.

Details from the source

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

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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