Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Liko Universal Twinbar 670 QRH Recalled by Baxter Healthcare Corporation Due to An incorrect center bolt was used in the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
Quantity: 1,399 twinbars
Why Was This Recalled?
An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report