Recall Z-2031-2025— Baxter Healthcare Corporation

Class I FDA medical device recall by Baxter Healthcare Corporation, initiated 2025-05-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift - Product Code 2040045A; 5) Viking S Mobile Lift - Product Code 2040006; 6) Viking XS Mobile Lift - Product Code 2040007; 7) LikoLight Mobile lift - Product Code 2030001. .. Reason: 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..

Recalling firm

Baxter Healthcare Corporation

Classification

Class I

Status

Ongoing

Initiated

2025-05-30

Firm location

Deerfield, IL, United States

Data sourced from openFDA. This site is unofficial and independent of the FDA.