Public recall detail

Liko Universal Twinbar 670 Qrh

medium
Recall Safety notice
Quick summary

Quick summary: Liko Universal Twinbar 670 Qrh.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Liko Universal Twinbar 670 Qrh.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandLiko Ab
ProductLiko Universal Twinbar 670 Qrh
IssueMedical devices - Manufacturing defect
Recall classType II
IdentificationRA-63968

Affected products

ProductLiko Universal Twinbar 670 Qrh
LotNot applicable.
Model3156087, P3156087
Serial numberNot applicable.
DescriptionLiko Universal Twinbar 670 Qrh

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesLiko Ab Nedre Vagen 100, Lulea Sweden, 97592
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63968
Background{}
CompaniesLiko Ab Nedre Vagen 100, Lulea Sweden, 97592
AudiencesGeneral public Health professionals Hospitals
Source updated2022-03-07

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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