The Recall Desk
Severity pendingFDA (Devices)·Z-2031-2025·Announced 2025-07-16

Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts:

Pending LLM rewrite. Source: FDA_DEVICE Z-2031-2025.

Severity not yet assessed

We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.

Plain-English summary

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.

The recalled product

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 -
Manufacturer
Baxter Healthcare Corporation
Category
Medical Device — Devices

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (12)

  • UDI/DI 00887761981775
  • 2) Product Code 2040044
  • UDI/DI 00887761981867
  • 3) Product Code 2040043
  • UDI/DI 00887761981850
  • 4) Product Code 2040045A
  • UDI/DI 00887761943193
  • 5) Product Code 2040006
  • UDI/DI N/A
  • 6) Product Code 2040007
  • 7) Product Code 2030001
  • UDI/DI N/A. .

Distribution

Distribution scope not specified by the agency.

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