Health product recall

Liko Universal Twinbar 670 Qrh

Brand(s)
Last updated

Summary

Product
Liko Universal Twinbar 670 Qrh
Issue
Medical devices - Manufacturing defect
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected Products

Lot or Serial Number

Model or catalog number

Liko Universal Twinbar 670 Qrh

Not applicable.

3156087, P3156087

Issue

During manufacturing of universal twinbar 670 Qrh, the wrong center bolt was used for some twinbars. The wrong bolt does, under some circumstances, prevent a rotation of the twinbar around its center bolt. When the rotation around the bolt is inhibited, a momentum is transferred to the attachment between the twinbar and the lift. This has caused breakage in the field resulting in patient falls. To date, there have been no reported injuries.

Recall start date: Feb 25. 2022

Additional information

Details
Original published date: 2022-03-09
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies

Liko Ab

Nedre Vagen 100, Lulea

Sweden, 97592

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63968