# FDA recall Z-0829-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-02-21.

## Product

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

## Reason for recall

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

## Distribution

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.

## Key facts

- **Recall number:** Z-0829-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-02-21
- **Report date:** 2022-04-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0829-2022

## Citation

> AI Analytics. FDA recall Z-0829-2022. Retrieved 2026-07-07 from https://api.ai-analytics.org/recall/Z-0829-2022. Source: US FDA. Licensed CC0.

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