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