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:
Alert / recall type
Health product recall
Category
Health products - Medical devices - 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
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