FDAClass IIFebruary 23, 2022

Liko Mobile Lifts: Primarily intended for use in recall

Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010

Why was Liko Mobile Lifts: Primarily intended for use in recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5

Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Recalling firm
Hill-Rom, Inc.
Quantity
5470 units
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.
Recall date
February 23, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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