Reported Jul 16, 2025 · Ongoing
Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile…
Baxter Healthcare Corporation
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625
Is this the product you have?
7 of 7 products
| Model / number | Product as published |
|---|---|
2010004 | Uno 102 EE Mobile lift |
2040044 | Viking L Mobile lift |
2040043 | Viking XL Mobile lift |
2040045A | Viking M Mobile lift |
2040006 | Viking S Mobile Lift |
2040007 | Viking XS Mobile Lift |
2030001. | LikoLight Mobile lift - . |
- Amount recalled
- 9899 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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