CLASS II ONGOING Device recall · Reported 6 Apr 2022 · FDA Enforcement Report

Liko Universal Twinbar 670 QRH recalled by Baxter Healthcare

Baxter Healthcare is recalling Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko, distributed nationwide in the US. The recall was initiated on 21 Feb 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesManufactured before 28OCT2021, UDI 00887761982468

Quantity recalled1,399 twinbars

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0829-2022
FDA event ID: 89598
Recalling firm: Baxter Healthcare, Deerfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 21 Feb 2022
FDA classified: 28 Mar 2022
Reported: 6 Apr 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

21 Feb 2022	Recall initiated by company
28 Mar 2022	Classified by FDA	+35 days
6 Apr 2022	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.

Product as listed by the FDA

Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.

Where it was distributed

Worldwide distribution - US Nationwide distribution in the states of AK, AZ, CA, CO, DC, FL, GA, HI, IA, ID, IN, KS, KY, LA, MA, MD, MI, MN, MO, ND, NE, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, and WI. There was government distribution but no military distribution. The countries of Austria, Australia, Brazil, Canada, Chile, China, Colombia, Denmark, Finland, France, Germany, Hong Kong, Ireland, Japan, Jordan, Latvia, Netherlands, Portugal, South Africa, Spain, Sweden, Switzerland, Taiwan, Tunisia, United Kingdom, and Uruguay.

Nationwide Alaska Arizona California Colorado District of Columbia Florida Georgia Hawaii Iowa Idaho Indiana Kansas Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri North Dakota

Questions about this recall

Why was it recalled?

An incorrect center bolt was used in the assembly of the product which could result in a patient fall during use.

Which lots are affected?

Manufactured before 28OCT2021, UDI 00887761982468

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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