Recall Z-0925-2021— Hill-Rom, Inc.

Class I FDA medical device recall by Hill-Rom, Inc., initiated 2020-12-18, terminated 2023-09-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal SlingBar 350 R2R (product number 3156094) Carriage D45 with Double Hook (product number 3136100) Extension belt 300-400 mm (product number 3136226) Extension belt 400-600 mm (product number 3136227) Extension belt 600-1000 mm (product number 3136228) Extension belt 1000-1400mm (product number 3136229). Reason: Multirall Q-link strap lock has not been fully engaged in the S65 rail carriage hook by user, leading to the Multirall lift becoming detached from the rail system, potentially resulting in the fall of both the lift motor and the patient.

Recalling firm

Hill-Rom, Inc.

Classification

Class I

Status

Terminated

Initiated

2020-12-18

Terminated

2023-09-26

Firm location

Batesville, IN, United States

Data sourced from openFDA. This site is unofficial and independent of the FDA.