Hill-Rom, Inc. Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
Brand
Hill-Rom, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Serial numbers: 5263715-5269464. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5
Hill-Rom, Inc. is recalling Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010 due to Missing bushing on Liko M220 and M230 causing wear and potential for patient falling. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Missing bushing on Liko M220 and M230 causing wear and potential for patient falling
Recommended Action
Per FDA guidance
HillRom issued Urgent Medical Device Correction Letter (FSCA Identifier: FA 2021-010-002-LUL-001) via third party on 23 December 2021 via UPS Ground Service to Distributors and Direct Users. Letter states reason for recall, health risk and action to take: 1. Review the product label on your Liko M220/M230 to determine if it is impacted by this field action by identifying the manufacturing date of the device (i.e. Manufacturing date between 2016-DEC-27 and 2021 SEP-01). See figure 2. 2. Please periodically inspect your Liko device for damage or wear. Report visible wearing or damage to your Technical Support Team do not use the device until Technical Support can inspect and repair where necessary. 3. Please fill out the attached response form and return it to Hillrom hillromLUL001@sedgwick.com within two weeks Please share this Field Safety Notice with your end users and complete the attached response form and return to hillromLUL001@sedgwick.com within two weeks. Contact hillromLUL001@sedgwick.com to receive an electronic copy of this notification and response form for onward distribution. Action to be taken by the Hillrom: Upon receipt of the response form, identifying potentially impacted devices, Hillrom or an official Hillrom distributor/representative will be in contact to schedule inspection of your device to confirm presence of the bushing. Where it is confirmed the device is missing the bushing, a replacement slingbar with the bushing will be installed. If you have any questions regarding this safety notice, please contact Hillrom Technical Support at 800-445-3720 or technical.support@hillrom.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026