CLASS II ONGOING Device recall · Reported 23 Feb 2022 · FDA Enforcement Report
Liko Mobile Lifts: Primarily intended for use recalled by Hill-Rom
Hill-Rom is recalling Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230, distributed nationwide in the US. The recall was initiated on 23 Dec 2021 and the FDA has classified it as Class II.
Check your package
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-0640-2022
- FDA event ID
- 89414
- Recalling firm
- Hill-Rom, Batesville, IN
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Dec 2021
- FDA classified
- 14 Feb 2022
- Reported
- 23 Feb 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 23 Dec 2021 | Recall initiated by company | |
| 14 Feb 2022 | Classified by FDA | +53 days |
| 23 Feb 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
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Product as listed by the FDA
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
Where it was distributed
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.
Questions about this recall
Why was it recalled?
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Which lots are affected?
Serial numbers: 5361393-5362761. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5
Where was it sold?
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.
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.
Other products in this recall event
1 other product · FDA event 89414| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Liko Mobile Lifts: Primarily intended for use recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
More recalls from Hill-Rom
All 37| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Traverse Rail Carrier E-System recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | Liko Mobile Lifts: Primarily intended for use recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | These are communication systems, labeled as recalled by Hill-Rom | Hill-Rom | Device Malfunction | Nationwide |
| Device | CLASS II | OctoStretch with Stretch Leveller recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
| Device | CLASS II | FlexoStretch Model Number recalled by Hill-Rom | Hill-Rom | Other | Nationwide |
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