Hillrom LikoScale component recall
Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code…
Why was Hillrom LikoScale component recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All LikoScale Adapter Kits manufactured between 8/27/2013 to 2/27/2025
- Product
- Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code…
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 9839 units
- Distribution
- Worldwide
- Recall date
- July 16, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)