Baxter Healthcare Corporation: Medical Device Recall in 2022 - (Recall #: Z-0829-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: February 21, 2022

Date Posted: April 6, 2022

Recall Number: Z-0829-2022

Event ID: 89598

Reason for Recall:

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

Status: Ongoing

Product Quantity: 1,399 twinbars

Code Information:

Manufactured before 28OCT2021, UDI 00887761982468

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated