Recall
FDAHealthMay 30, 2025

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) L

⚠️ 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.

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
May 30, 2025

Worldwide

What's affected?

Product
Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
Lot code
All LikoScale Adapter Kits manufactured between 8/27/2013 to 2/27/2025

Additional details

All LikoScale Adapter Kits manufactured between 8/27/2013 to 2/27/2025

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 9839 units.

View original FDA notice →

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