# FDA recall Z-2031-2025

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2025-05-30.

## 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 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

## Key facts

- **Recall number:** Z-2031-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-30
- **Report date:** 2025-07-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2031-2025

## Citation

> AI Analytics. FDA recall Z-2031-2025. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2031-2025. Source: US FDA. Licensed CC0.

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