Health product recall

LikoGuard L and LikoGuard XL (2017-12-18)

Starting date:
December 18, 2017
Posting date:
January 29, 2018
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-65798

Affected products

LikoGuard L and LikoGuard XL

Reason

Over time a plastic component internal of the lift may deform; therefore reducing the functionality of the back-up mechanical lowering feature to almost non-functional.

Affected products

LikoGuard L and LikoGuard XL

Lot or serial number

Not applicable

Model or catalog number
  • 3301030
  • 3301040
Companies
Manufacturer
Liko AB
Nedre Vagen 100
Lulea
97592
SWEDEN