# FDA recall Z-0640-2022

> **Hill-Rom, Inc.** · Class II · device recall initiated 2021-12-23.

## Product

Liko Mobile Lifts: Primarily intended for use in nursing homes  LikoM230	Model: 2050015

## Reason for recall

Missing bushing on Liko M220 and M230 causing wear and potential for patient falling

## Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Austria, Bahrain,  Canada, Switzerland, Germany, Denmark, Spain, Finland, France, United Kingdom,  Greece, Hong Kong, Ireland, Israel, Italy, Norway, Saudi Arabia, Sweden, Slovenia,  Taiwan (Province of China), South Africa, Oman.

## Key facts

- **Recall number:** Z-0640-2022
- **Recalling firm:** Hill-Rom, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-12-23
- **Report date:** 2022-02-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Batesville, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0640-2022

## Citation

> AI Analytics. FDA recall Z-0640-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0640-2022. Source: US FDA. Licensed CC0.

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