Liko Mobile Lifts: Primarily intended for use in recall
Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
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: 5361393-5362761. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5
- Product
- Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015
- Recalling firm
- Hill-Rom, Inc.
- Quantity
- 1215 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)