Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

FDA Recall #Z-0640-2022 — Class II — December 23, 2021

Recall #Z-0640-2022 Date: December 23, 2021 Classification: Class II Status: Ongoing

Product Description

Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015

Reason for Recall

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

Recalling Firm

Hill-Rom, Inc. — Batesville, IN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product 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.

Code Information

Serial numbers: 5361393-5362761. Manufactured between 2016-DEC-27 and 2021-SEP-01. UDI: 0887761GMN000034U5

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated