---
title: "Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Mod... — FDA record Z-0639-2022 | Is It on Recall"
description: "Missing bushing on Liko M220 and M230 causing wear and potential for patient falling"
url: https://isitonrecall.com/recall/fda-device-z-0639-2022-liko-mobile-lifts-primarily-intended-for-use-in-nursing-homes-liko-m220-model-2050010/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010 — FDA record Z-0639-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 23, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
- **Reason**: Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
- **Classification**: Class II
- **Recalling firm**: Hill-Rom, Inc.
- **Quantity**: 5470 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0639-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0639-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Feb 23, 2022
- **Recall initiation date**: Dec 23, 2021
- **Center classification date**: Feb 14, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0639-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Hill-Rom Inc. records](https://isitonrecall.com/brand/hill-rom-inc/)
